Common Variable Immunodeficiency with Genetic Defects Identified by Whole Exome Sequencing

Common variable immunodeficiency (CVID) belongs to the primary immunodeficiency disorders (PIDs), presenting a profound heterogeneity in phenotype and genotype, with monogenic or complex causes. Recurrent respiratory infections are the most common clinical manifestations. CVID patients can also deve...

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Detalles Bibliográficos
Autores principales: Li, Ran, Zheng, Yali, Li, Yuqian, Zhang, Rongbao, Wang, Fang, Yang, Donghong, Ma, Yanliang, Mu, Xinlin, Cao, Zhaolong, Gao, Zhancheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186323/
https://www.ncbi.nlm.nih.gov/pubmed/30363934
http://dx.doi.org/10.1155/2018/3724630

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186323/
https://www.ncbi.nlm.nih.gov/pubmed/30363934
http://dx.doi.org/10.1155/2018/3724630

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