Genomic organization and structure of Bruton agammaglobulinemia tyrosine kinase: localization of mutations associated with varied clinical presentations and course in X chromosome-linked agammaglobulinemia.

X chromosome-linked agammaglobulinemia is a life-threatening disease that involves a failure in normal development of B lymphocytes and is associated with missense mutations in BTK, a gene encoding a cytoplasmic tyrosine kinase (Bruton agammaglobulinemia tyrosine kinase, EC 2.7.1.112), a member of t...

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Enregistré dans:
Détails bibliographiques
Auteurs principaux: Ohta, Y, Haire, R N, Litman, R T, Fu, S M, Nelson, R P, Kratz, J, Kornfeld, S J, de la Morena, M, Good, R A, Litman, G W
Format: Artigo
Langue:Inglês
Publié: 1994
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC44747/
https://ncbi.nlm.nih.gov/pubmed/8090769
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