LRRC8Abase: Non-Bruton type autosomal dominant agammaglobulinemia

Version 1.0 last updated 18 June, 2007 contains 1 public entries


Curated:	Mauno Vihinen
Maintained by:	Jouni Väliaho
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Short description of the LRRC8Abase :

A chromosomal aberration involving LRRC8 is a cause of non-bruton type agammaglobulinemia. Agammaglobulinemia is an immunodeficiency disease which results in developmental defects in the maturation pathway of B-cells.

Other resourses:
Immunodeficiency Resource (IDR)
Immunodeficiency Mutation Databases (MUTbase)
IDdiagnostics

IDbases are linked to University of California Santa Cruz (UCSC) genome browser: LRRC8Abase