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Clinical characteristics and genetic profiles of 174 patients with X-linked agammaglobulinemia: Report from Shanghai, China (2000–2015)

X-linked agammaglobulinemia (XLA) is a humoral primary immunodeficiency. XLA patients typically present with very low numbers of peripheral B cells and a profound deficiency of all immunoglobulin isotypes. Most XLA patients carry mutations in Bruton tyrosine kinase (BTK) gene. The genetic background...

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Detalles Bibliográficos
Autores principales:	Chen, Xia-Fang, Wang, Wei-Fan, Zhang, Yi-Dan, Zhao, Wei, Wu, Jing, Chen, Tong-Xin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2016
Materias:	3600
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985333/ https://www.ncbi.nlm.nih.gov/pubmed/27512878 http://dx.doi.org/10.1097/MD.0000000000004544

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