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- databases for immunodeficiency-causing variations

   LRRC8Abase
   Variation registry for  Non-Bruton type autosomal dominant agammaglobulinemia


LRRC8Abase mutation publications

[2003]

Search PubMed latest citations for LRRC8A mutations

    2003

  • A congenital mutation of the novel gene LRRC8 causes agammaglobulinemia in humans.
    Sawada A, Takihara Y, Kim JY, Matsuda-Hashii Y, Tokimasa S, Fujisaki H, Kubota K, Endo H, Onodera T, Ohta H, Ozono K, Hara J
    J Clin Invest 2003(11): 1707-13 [PubMed abstract].