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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Kanegane, H, Tsukada, S, Iwata, T, Futatani, T, Nomura, K, Yamamoto, J, Yoshida, T, Agematsu, K, Komiyama, A, Miyawaki, T
Formato: Artigo
Lenguaje:Inglês
Publicado: Blackwell Science Inc 2000
Materias:
Immunodeficiency
Acceso en línea: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
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares