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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Dades bibliogràfiques
Publicat a:Front Immunol
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2020
Matèries:
Immunology
Accés en línia: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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