BTKbase, mutation database for X-linked agammaglobulinemia (XLA)

X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by mutations in the gene coding for Bruton's agammaglobulinemia tyrosine kinase (BTK). A database (BTKbase) of BTK mutations has been compiled and the recent update lists 368 entries from 318 unrelated families showing 228 unique m...

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Autors principals: Vihinen, M, Belohradsky, B H, Haire, R N, Holinski-Feder, E, Kwan, S P, Lappalainen, I, Lehväslaiho, H, Lester, T, Meindl, A, Ochs, H D, Ollila, J, Vorechovsky, I, Weiss, M, Smith, C I
Format: Artigo
Idioma:Inglês
Publicat: 1997
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC146405/
https://ncbi.nlm.nih.gov/pubmed/9016530
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