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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Biomed Res Int
Autors principals: Li, Ran, Zheng, Yali, Li, Yuqian, Zhang, Rongbao, Wang, Fang, Yang, Donghong, Ma, Yanliang, Mu, Xinlin, Cao, Zhaolong, Gao, Zhancheng
Format: Artigo
Idioma:Inglês
Publicat: Hindawi 2018
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6186323/
https://ncbi.nlm.nih.gov/pubmed/30363934
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/3724630
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars