Kinase mutant Btk results in atypical X-linked agammaglobulinaemia phenotype

X-linked agammaglobulinaemia (XLA) is a B cell humoral abnormality arising from mutations in the gene encoding Bruton's tyrosine kinase (Btk). The phenotype of XLA can be variable, with some individuals having a less severe immunophenotype, although in most cases this cannot be correlated with...

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Detalhes bibliográficos
Main Authors: Gaspar, H B, Ferrando, M, Caragol, I, Hernandez, M, Bertran, J M, De Gracia, X, Lester, T, Kinnon, C, Ashton, E, Espanol, T
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Science Inc 2000
Assuntos:
Immunodeficiency
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1905636/
https://ncbi.nlm.nih.gov/pubmed/10792386
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2249.2000.01230.x
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