Distinct Clinical Features and Novel Mutations in Taiwanese Patients With X-Linked Agammaglobulinemia

Background: X-linked agammaglobulinemia (XLA) is caused by a mutation of the Bruton's tyrosine kinase (BTK) gene and is the most common genetic mutation in patients with congenital agammaglobulinemia. The aim of this study was to analyze the clinical features, genetic defects, and/or BTK expres...

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Detalles Bibliográficos
Publicado en:Front Immunol
Main Authors: Yeh, Yu-Hsin, Hsieh, Meng-Ying, Lee, Wen-I, Huang, Jing-Long, Chen, Li-Chen, Yeh, Kuo-Wei, Ou, Liang-Shiou, Yao, Tsung-Chieh, Wu, Chao-Yi, Lin, Syh-Jae
Formato: Artigo
Idioma:Inglês
Publicado: Frontiers Media S.A. 2020
Assuntos:
Immunology
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7498534/
https://ncbi.nlm.nih.gov/pubmed/33013854
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2020.02001
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