Online Mendelian Inheritance in Man (OMIM) (2024)

  1. Berning, A. K., Eicher, E. M., Paul, W. E., Scher, I. Mapping of the X-linked immune deficiency mutation (xid) of CBA/N mice. J. Immun. 124: 1875-1877, 1980. [PubMed: 7365241]

  2. Bradley, L. A. D., Sweatman, A. K., Lovering, R. C., Jones, A. M., Morgan, G., Levinsky, R. J., Kinnon, C. Mutation detection in the X-linked agammaglobulinemia gene, BTK, using single strand conformation polymorphism analysis. Hum. Molec. Genet. 3: 79-83, 1994. [PubMed: 8162056] [Full Text: https://doi.org/10.1093/hmg/3.1.79]

  3. Buckley, R. H., Rowlands, D. T., Jr. Agammaglobulinemia, neutropenia, fever, and abdominal pain. J. Allergy Clin. Immun. 51: 308-318, 1973. [PubMed: 4697357] [Full Text: https://doi.org/10.1016/0091-6749(73)90133-4]

  4. Buckley, R. H. Assessing inheritance of agammaglobulinemia. (Editorial) New Eng. J. Med. 330: 1526-1528, 1994. [PubMed: 8164707] [Full Text: https://doi.org/10.1056/NEJM199405263302111]

  5. Bykowsky, M. J., Haire, R. N., Ohta, Y., Tang, H., Sung, S.-S. J., Veksler, E. S., Greene, J. M., Fu, S. M., Litman, G. W., Sullivan, K. E. Discordant phenotype in siblings with X-linked agammaglobulinemia. Am. J. Hum. Genet. 58: 477-483, 1996. [PubMed: 8644706]

  6. Cheng, G., Ye, Z.-S., Baltimore, D. Binding of Bruton's tyrosine kinase to Fyn, Lyn, or Hck through a Src hom*ology 3 domain-mediated interaction. Proc. Nat. Acad. Sci. 91: 8152-8155, 1994. [PubMed: 8058772] [Full Text: https://doi.org/10.1073/pnas.91.17.8152]

  7. Cohen, D. I., Steinberg, A. D., Paul, W. E., Davis, M. M. Expression of an X-linked gene family (XLR) in late-stage B cells and its alteration by the xid mutation.. Nature 314: 372-374, 1985. [PubMed: 3872416] [Full Text: https://doi.org/10.1038/314372a0]

  8. Conley, M. E., Burks, A. W., Herrod, H. G., Puck, J. M. Molecular analysis of X-linked agammaglobulinemia with growth hormone deficiency. J. Pediat. 119: 392-397, 1991. [PubMed: 1880652] [Full Text: https://doi.org/10.1016/s0022-3476(05)82051-7]

  9. Conley, M. E., Fitch-Hilgenberg, M. E., Cleveland, J. L., Parolini, O., Rohrer, J. Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase. Hum. Molec. Genet. 3: 1751-1756, 1994. [PubMed: 7849697] [Full Text: https://doi.org/10.1093/hmg/3.10.1751]

  10. Conley, M. E., Mathias, D., Treadaway, J., Minegishi, Y., Rohrer, J. Mutations in Btk in patients with presumed X-linked agammaglobulinemia. Am. J. Hum. Genet. 62: 1034-1043, 1998. [PubMed: 9545398] [Full Text: https://doi.org/10.1086/301828]

  11. Conley, M. E., Puck, J. M. Carrier detection in typical and atypical X-linked agammaglobulinemia. J. Pediat. 112: 688-694, 1988. [PubMed: 2896233] [Full Text: https://doi.org/10.1016/s0022-3476(88)80683-8]

  12. Curtis, S. K., Hebert, M. D., Saha, B. K. Twin carriers of X-linked agammaglobulinemia (XLA) due to germline mutation in the Btk gene. Am. J. Med. Genet. 90: 229-232, 2000. [PubMed: 10678660] [Full Text: https://doi.org/10.1002/(sici)1096-8628(20000131)90:3<229::aid-ajmg8>3.0.co;2-q]

  13. de Weers, M., Mensink, R. G. J., Kraakman, M. E. M., Schuurman, R. K. B., Hendriks, R. W. Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid mice. Hum. Molec. Genet. 3: 161-166, 1994. [PubMed: 8162018] [Full Text: https://doi.org/10.1093/hmg/3.1.161]

  14. Desiderio, S. Becoming B cells. (Abstract) Nature 361: 202, 1993.

    See Also
    X-Linked Agammaglobulinemia in Children | University HospitalsX-Linked Agammaglobulinemia in ChildrenDirect and Indirect Costs of Immunoglobulin Replacement Therapy in Patients with Common Variable Immunodeficiency (CVID) and X-Linked Agammaglobulinemia (XLA) in Italy.X-Linked Agammaglobulinemia in Children

  15. Drabek, D., Raguz, S., De Wit, T. P. M., Dingjan, G. M., Savelkoul, H. F. J., Grosveld, F., Hendriks, R. W. Correction of the X-linked immunodeficiency phenotype by transgenic expression of human Bruton tyrosine kinase under the control of the class II major histocompatibility complex Ea locus control region. Proc. Nat. Acad. Sci. 94: 610-615, 1997. [PubMed: 9012832] [Full Text: https://doi.org/10.1073/pnas.94.2.610]

  16. Duriez, B., Duquesnoy, P., Dastot, F., Bougneres, P., Amselem, S., Goossens, M. An exon-skipping mutation in the btk gene of a patient with X-linked agammaglobulinemia and isolated growth hormone deficiency. FEBS Lett. 346: 165-170, 1994. [PubMed: 8013627] [Full Text: https://doi.org/10.1016/0014-5793(94)00457-9]

  17. Hagemann, T. L., Chen, Y., Rosen, F. S., Kwan, S.-P. Genomic organization of the Btk gene and exon scanning for mutations in patients with X-linked agammaglobulinemia. Hum. Molec. Genet. 3: 1743-1749, 1994. [PubMed: 7880320] [Full Text: https://doi.org/10.1093/hmg/3.10.1743]

  18. Hagemann, T. L., Rosen, F. S., Kwan, S.-P. Characterization of germline mutations of the gene encoding Bruton's tyrosine kinase in families with X-linked agammaglobulinemia. Hum. Mutat. 5: 296-302, 1995. [PubMed: 7627183] [Full Text: https://doi.org/10.1002/humu.1380050405]

  19. Hantschel, O., Rix, U., Schmidt, U., Burckstummer, T., Kneidinger, M., Schutze, G., Colinge, J., Bennett, K. L., Ellmeier, W., Valent, P., Superti-Furga, G. The Btk tyrosine kinase is a major target of the Bcr-Abl inhibitor dasatinib. Proc. Nat. Acad. Sci. 104: 13283-13288, 2007. [PubMed: 17684099] [Full Text: https://doi.org/10.1073/pnas.0702654104]

  20. Hasan, M., Lopez-Herrera, G., Blomberg, K. E. M., Lindvall, J. M., Berglof, A., Smith, C. I. E., Vargas, L. Defective Toll-like receptor 9-mediated cytokine production in B cells from Bruton's tyrosine kinase-deficient mice. Immunology 123: 239-249, 2007. [PubMed: 17725607] [Full Text: https://doi.org/10.1111/j.1365-2567.2007.02693.x]

  21. Jo, E.-K., Kanegane, H., Nonoyama, S., Tsukada, S., Lee, J.-H., Lim, K., Shong, M., Song, C.-H., Kim, H.-J., Park, J.-K., Miyawaki, T. Characterization of mutations, including a novel regulatory defect in the first intron, in Bruton's tyrosine kinase gene from seven Korean X-linked agammaglobulinemia families. J. Immun. 167: 4038-4045, 2001. [PubMed: 11564824] [Full Text: https://doi.org/10.4049/jimmunol.167.7.4038]

  22. Jo, E.-K., Wang, Y., Kanegane, H., Futatani, T., Song, C.-H., Park, J.-K., Kim, J. S., Kim, D. S., Ahn, K.-M., Lee, S.-I., Park, H. J., Hahn, Y. S., Lee, J.-H., Miyawaki, T. Identification of mutations in the Bruton's tyrosine kinase gene, including a novel genomic rearrangements (sic) resulting in large deletion, in Korean X-linked agammaglobulinemia patients. J. Hum. Genet. 48: 322-326, 2003. [PubMed: 12768435] [Full Text: https://doi.org/10.1007/s10038-003-0032-4]

  23. Jones, A., Bradley, L., Alterman, L., Tarlow, M., Thompson, R., Kinnon, C., Morgan, G. X linked agammaglobulinaemia with a 'leaky' phenotype. Arch. Dis. Child. 74: 548-549, 1996. [PubMed: 8758136] [Full Text: https://doi.org/10.1136/adc.74.6.548]

  24. Kawakami, Y., Inagaki, N., Salek-Ardakani, S., Kitaura, J., Tanaka, H., Nagao, K., Kawakami, Y., Xiao, W., Nagai, H., Croft, M., Kawakami, T. Regulation of dendritic cell maturation and function by Bruton's tyrosine kinase via IL-10 and Stat3. Proc. Nat. Acad. Sci. 103: 153-158, 2006. [PubMed: 16371463] [Full Text: https://doi.org/10.1073/pnas.0509784103]

  25. Kobayashi, S., Iwata, T., Saito, M., Iwasaki, R., Matsumoto, H., Naritaka, S., Kono, Y., Hayashi, Y. Mutations of the Btk gene in 12 unrelated families with X-linked agammaglobulinemia in Japan. Hum. Genet. 97: 424-430, 1996. [PubMed: 8834236]

  26. Kornfeld, S. J., Kratz, J., Haire, R. N., Litman, G. W., Good, R. A. X-linked agammaglobulinemia presenting as transient hypogammaglobulinemia of infancy. J. Allergy Clin. Immun. 95: 915-917, 1995. [PubMed: 7722175] [Full Text: https://doi.org/10.1016/s0091-6749(95)70138-9]

  27. Mao, C., Zhou, M., Uckun, F. M. Crystal structure of Bruton's tyrosine kinase domain suggests a novel pathway for activation and provides insights into the molecular basis of X-linked agammaglobulinemia. J. Biol. Chem. 276: 41435-41443, 2001. [PubMed: 11527964] [Full Text: https://doi.org/10.1074/jbc.M104828200]

  28. Mao, L., Kitani, A., Hiejima, E., Montgomery-Recht, K., Zhou, W., Fuss, I., Wiestner, A., Strober, W. Bruton tyrosine kinase deficiency augments NLRP3 inflammasome activation and causes IL-1-beta-mediated colitis. J. Clin. Invest. 130: 1793-1807, 2020. [PubMed: 31895698] [Full Text: https://doi.org/10.1172/JCI128322]

    See Also
    Primary immunodeficiency diseases : a molecular and genetic approach / edited by Hans D. Ochs, C.I. Edvard Smith, Jennifer M. Puck

  29. Marshall-Clarke, S., Cooke, A., Hutchings, P. R. Deficient production of anti-red cell autoantibodies by mice with an X-linked B-lymphocyte defect. Europ. J. Immun. 9: 820-823, 1979. [PubMed: 316393] [Full Text: https://doi.org/10.1002/eji.1830091014]

  30. Martin, S., Wolf-Eichbaum, D., Duinkerken, G., Scherbaum, W. A., Kolb, H., Noordzij, J. G., Roep, B. O. Development of type 1 diabetes despite severe hereditary B-cell deficiency. New Eng. J. Med. 345: 1036-1040, 2001. [PubMed: 11586956] [Full Text: https://doi.org/10.1056/NEJMoa010465]

  31. Minegishi, Y., Coustan-Smith, E., Wang, Y.-H., Cooper, M. D., Campana, D., Conley, M. E. Mutations in the human lambda-5/14.1 gene result in B cell deficiency and agammaglobulinemia. J. Exp. Med. 187: 71-77, 1998. [PubMed: 9419212] [Full Text: https://doi.org/10.1084/jem.187.1.71]

  32. Ng, Y.-S., Wardemann, H., Chelnis, J., Cunningham-Rundles, C., Meffre, E. Bruton's tyrosine kinase is essential for human B cell tolerance. J. Exp. Med. 200: 927-934, 2004. [PubMed: 15466623] [Full Text: https://doi.org/10.1084/jem.20040920]

  33. Oeltjen, J. C., Liu, X., Lu, J., Allen, R. C., Muzny, D., Belmont, J. W., Gibbs, R. A. Sixty-nine kilobases of contiguous human genomic sequence containing the alpha-galactosidase A and Bruton's tyrosine kinase loci. Mammalian Genome 6: 334-338, 1995. [PubMed: 7626884] [Full Text: https://doi.org/10.1007/BF00364796]

  34. Ohta, Y., Haire, R. N., Litman, R. T., Fu, S. M., Nelson, R. P., Kratz, J., Kornfeld, S. J., de la Morena, M., Good, R. A., Litman, G. W. Genomic organization and structure of Bruton agammaglobulinemia tyrosine kinase: localization of mutations associated with varied clinical presentations and course in X chromosome-linked agammaglobulinemia. Proc. Nat. Acad. Sci. 91: 9062-9066, 1994. [PubMed: 8090769] [Full Text: https://doi.org/10.1073/pnas.91.19.9062]

  35. Parolini, O., Hejtmancik, J. F., Allen, R. C., Belmont, J. W., Lassiter, G. L., Henry, M. J., Barker, D. F., Conley, M. E. Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22. Genomics 15: 342-349, 1993. [PubMed: 8449500] [Full Text: https://doi.org/10.1006/geno.1993.1066]

  36. Rawlings, D. J., Saffran, D. C., Tsukada, S., Largaespada, D. A., Grimaldi, J. C., Cohen, L., Mohr, R. N., Bazan, J. F., Howard, M., Copeland, N. G., Jenkins, N. A., Witte, O. N. Mutation of unique region of Bruton's tyrosine kinase in immunodeficient xid mice. Science 261: 358-361, 1993. [PubMed: 8332901] [Full Text: https://doi.org/10.1126/science.8332901]

  37. Rawlings, D. J., Witte, O. N. Bruton's tyrosine kinase is a key regulator in B-cell development. Immun. Rev. 138: 105-119, 1994. [PubMed: 8070812] [Full Text: https://doi.org/10.1111/j.1600-065x.1994.tb00849.x]

  38. Rohrer, J., Parolini, O., Belmont, J. W., Conley, M. E. The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia. Immunogenetics 40: 319-324, 1994. Note: Erratum: Immunogenetics 42: 76 only, 1995. [PubMed: 7927535] [Full Text: https://doi.org/10.1007/BF01246672]

  39. Saffran, D. C., Parolini, O., Fitch-Hilgenberg, M. E., Rawlings, D. J., Afar, D. E. H., Witte, O. N., Conley, M. E. A point mutation in the SH2 domain of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia. New Eng. J. Med. 330: 1488-1491, 1994. [PubMed: 8164701] [Full Text: https://doi.org/10.1056/NEJM199405263302104]

  40. Sakamoto, M., Kanegane, H., Fujii, H., Tsukada, S., Miyawaki, T., Shinomiya, N. Maternal germinal mosaicism of X-linked agammaglobulinemia. Am. J. Med. Genet. 99: 234-237, 2001. [PubMed: 11241495] [Full Text: https://doi.org/10.1002/1096-8628(2001)9999:9999<::aid-ajmg1159>3.0.co;2-m]

  41. Scher, I., Steinberg, A. D., Berning, A. K., Paul, W. E. X-linked B-lymphocyte immune defect in CBA-N mice. II. Studies of the mechanisms underlying the immune defect. J. Exp. Med. 142: 637-650, 1975. [PubMed: 1080788] [Full Text: https://doi.org/10.1084/jem.142.3.637]

  42. Shinohara, M., Koga, T., Okamoto, K., Sakaguchi, S., Arai, K., Yasuda, H., Takai, T., Kodama, T., Morio, T., Geha, R. S., Kitamura, D., Kurosaki, T., Ellmeier, W., Takayanagi, H. Tyrosine kinases Btk and Tec regulate osteoclast differentiation by linking RANK and ITAM signals. Cell 132: 794-806, 2008. [PubMed: 18329366] [Full Text: https://doi.org/10.1016/j.cell.2007.12.037]

  43. Thomas, J. D., Sideras, P., Smith, C. I. E., Vorechovsky, I., Chapman, V., Paul, W. E. Colocalization of X-linked agammaglobulinemia and X-linked immunodeficiency genes. Science 261: 355-358, 1993. [PubMed: 8332900] [Full Text: https://doi.org/10.1126/science.8332900]

  44. Tsukada, S., Saffran, D. C., Rawlings, D. J., Parolini, O., Allen, R. C., Klisak, I., Sparkes, R. S., Kubagawa, H., Mohandas, T., Quan, S., Belmont, J. W., Cooper, M. D., Conley, M. E., Witte, O. N. Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia. Cell 72: 279-290, 1993. [PubMed: 8425221] [Full Text: https://doi.org/10.1016/0092-8674(93)90667-f]

  45. Uckun, F. M., Waddick, K. G., Mahajan, S., Jun, X., Takata, M., Bolen, J., Kurosaki, T. BTK as a mediator of radiation-induced apoptosis in DT-40 lymphoma B cells. Science 273: 1096-1099, 1996. [PubMed: 8688094] [Full Text: https://doi.org/10.1126/science.273.5278.1096]

  46. van der Meer, J. W. M., Mouton, R. P., Daha, M. R., Schuurman, R. K. B. Campylobacter jejuni bacteraemia as a cause of recurrent fever in a patient with hypogammaglobulinaemia. J. Infect. 12: 235-239, 1986. [PubMed: 3722839] [Full Text: https://doi.org/10.1016/s0163-4453(86)94190-3]

  47. van Zelm, M. C., Geertsema, C., Nieuwenhuis, N., de Ridder, D., Conley, M. E., Schiff, C., Tezcan, I., Bernatowska, E., Hartwig, N. G., Sanders, E. A. M., Litzman, J., Kondratenko, I., van Dongen, J. J. M., van der Burg, M. Gross deletions involving IGHM, BTK, or Artemis: a model for genomic lesions mediated by transposable elements. Am. J. Hum. Genet. 82: 320-332, 2008. [PubMed: 18252213] [Full Text: https://doi.org/10.1016/j.ajhg.2007.10.011]

  48. Vetrie, D., Vorechovsky, I., Sideras, P., Holland, J., Davies, A., Flinter, F., Hammarstrom, L., Kinnon, C., Levinsky, R., Bobrow, M., Smith, C. I. E., Bentley, D. R. The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases. Nature 361: 226-233, 1993. Note: Erratum: Nature 364: 362 only, 1993. [PubMed: 8380905] [Full Text: https://doi.org/10.1038/361226a0]

  49. Vihinen, M., Iwata, T., Kinnon, C., Kwan, S.-P., Ochs, H. D., Vorechovsky, I., Smith, C. I. E. BTKbase, mutation database for X-linked agammaglobulinemia (XLA). Nucleic Acids Res. 24: 160-165, 1996. [PubMed: 8594569] [Full Text: https://doi.org/10.1093/nar/24.1.160]

  50. Vihinen, M., Kwan, S.-P., Lester, T., Ochs, H. D., Resnick, I., Valiaho, J., Conley, M. E., Smith, C. I. E. Mutations of the human BTK gene coding for Bruton tyrosine kinase in X-linked agammaglobulinemia. Hum. Mutat. 13: 280-285, 1999. [PubMed: 10220140] [Full Text: https://doi.org/10.1002/(SICI)1098-1004(1999)13:4<280::AID-HUMU3>3.0.CO;2-L]

  51. Vihinen, M., Vetrie, D., Maniar, H. S., Ochs, H. D., Zhu, Q., Vorechovsky, I., Webster, A. D. B., Notarangelo, L. D., Nilsson, L., Sowadski, J. M., Smith, C. I. E. Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease. Proc. Nat. Acad. Sci. 91: 12803-12807, 1994. [PubMed: 7809124] [Full Text: https://doi.org/10.1073/pnas.91.26.12803]

  52. Vorechovsky, I., Luo, L., Hertz, J. M., Froland, S. S., Klemola, T., Fiorini, M., Quinti, I., Paganelli, R., Ozsahin, H., Hammarstrom, L., Webster, A. D. B., Smith, C. I. E. Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X-linked agammaglobulinemia. Hum. Mutat. 9: 418-425, 1997. [PubMed: 9143921] [Full Text: https://doi.org/10.1002/(SICI)1098-1004(1997)9:5<418::AID-HUMU7>3.0.CO;2-#]

  53. Vorechovsky, I., Zhou, J.-N., Hammarstrom, L., Smith, C. I. E., Thomas, J. D., Paul, W. E., Notarangelo, L. D., Bernatowska-Matuszkiewicz, E. Absence of xid mutation in X-linked agammaglobulinaemia. (Letter) Lancet 342: 552, 1993. [PubMed: 8102684] [Full Text: https://doi.org/10.1016/0140-6736(93)91676-d]

  54. Vorechovsky, I., Zhou, J.-N., Vetrie, D., Bentley, D., Bjorkander, J., Hammarstrom, L., Smith, C. I. E. Molecular diagnosis of X-linked agammaglobulinaemia. (Letter) Lancet 341: 1153, 1993. Note: Erratum: Lancet 361: 1394 only, 2003. [PubMed: 8097835] [Full Text: https://doi.org/10.1016/0140-6736(93)93172-w]

  55. Wattanasirichaigoon, D., Benjaponpitak, S., Techasaensiri, C., Kamchaisatian, W., Vichyanond, P., Janwityanujit, S., Choubtum, L., Sirinavin, S. Four novel and three recurrent mutations of the BTK gene and pathogenic effects of putative splice mutations. J. Hum. Genet. 51: 1006-1014, 2006. [PubMed: 16951917] [Full Text: https://doi.org/10.1007/s10038-006-0052-y]

  56. Wood, P. M. D., Mayne, A., Joyce, H., Smith, C. I. E., Granoff, D. M., Kumararatne, D. S. A mutation in Bruton's tyrosine kinase as a cause of selective anti-polysaccharide antibody deficiency. J. Pediat. 139: 148-151, 2001. [PubMed: 11445810] [Full Text: https://doi.org/10.1067/mpd.2001.115970]

  57. Yel, L., Minegishi, Y., Coustan-Smith, E., Buckley, R. H., Trubel, H., Pachman, L. M., Kitchingman, G. R., Campana, D., Rohrer, J., Conley, M. E. Mutations in the mu heavy-chain gene in patients with agammaglobulinemia. New Eng. J. Med. 335: 1486-1493, 1996. [PubMed: 8890099] [Full Text: https://doi.org/10.1056/NEJM199611143352003]

  58. Zhu, Q., Zhang, M., Winkelstein, J., Chen, S.-H., Ochs, H. D. Unique mutations of Bruton's tyrosine kinase in fourteen unrelated X-linked agammaglobulinemia families. Hum. Molec. Genet. 3: 1899-1900, 1994. [PubMed: 7849721] [Full Text: https://doi.org/10.1093/hmg/3.10.1899]

Online Mendelian Inheritance in Man (OMIM) (2024)
Top Articles
Los San Francisco 49ers Revelan Su Calendario Completo Para la Temporada 2024
D18-410 Northfield Drive W, Waterloo, ON, N2L 0A6 - maison à vendre | No. Inscription 40590058
Apple Intelligence is free, but premium AI features may need a paid subscription
Democrats are talking about replacing Joe Biden. That wouldn't be so easy.
Peptides and scaffolds for use in immunotherapy against head and neck squamous cell carcinoma and other cancers
What Is Culver's Flavor Of The Day
Aimsweb Und
Craigslist Rvs For Sale By Owner Near Me
The state of AI in early 2024: Gen AI adoption spikes and starts to generate value
Tax Topic 152: Will I Still Get My Tax Refund?
Don't Skip These Video Games: 8 Hot Titles You Should Buy in July
Explore Skip The Game El Paso: Unlock Endless Fun!
Latest Posts
The best prescription sunglasses for 2024
The Effects of Prohibitions Associated with Domestic Violence
Article information

Author: Duane Harber

Last Updated:

Views: 5901

Rating: 4 / 5 (51 voted)

Reviews: 82% of readers found this page helpful

Author information

Name: Duane Harber

Birthday: 1999-10-17

Address: Apt. 404 9899 Magnolia Roads, Port Royceville, ID 78186

Phone: +186911129794335

Job: Human Hospitality Planner

Hobby: Listening to music, Orienteering, Knapping, Dance, Mountain biking, Fishing, Pottery

Introduction: My name is Duane Harber, I am a modern, clever, handsome, fair, agreeable, inexpensive, beautiful person who loves writing and wants to share my knowledge and understanding with you.