Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry

CVID is frequently diagnosed in male and female individuals with hypogammaglobulinaemia of unknown aetiology. To examine the possibility that sporadic male cases with X-linked agammaglobulinaemia (XLA), which is caused by mutations in the Bruton's tyrosine kinase (Btk) gene, might be misregiste...

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Detalhes bibliográficos
Main Authors: Kanegane, H, Tsukada, S, Iwata, T, Futatani, T, Nomura, K, Yamamoto, J, Yoshida, T, Agematsu, K, Komiyama, A, Miyawaki, T
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Science Inc 2000
Assuntos:
Immunodeficiency
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1905560/
https://ncbi.nlm.nih.gov/pubmed/10844531
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2249.2000.01244.x
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