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
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498534/
https://www.ncbi.nlm.nih.gov/pubmed/33013854
http://dx.doi.org/10.3389/fimmu.2020.02001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498534/
https://www.ncbi.nlm.nih.gov/pubmed/33013854
http://dx.doi.org/10.3389/fimmu.2020.02001

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