Recent advances in elucidating the genetics of common variable immunodeficiency

Common variable immunodeficiency disorders (CVID), a heterogeneous group of inborn errors of immunity, is the most common symptomatic primary immunodeficiency disorder. Patients with CVID have highly variable clinical presentation. With the advent of whole genome sequencing and genome wide associati...

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Detalles Bibliográficos
Autores principales: Aggarwal, Vaishali, Banday, Aaqib Zaffar, Jindal, Ankur Kumar, Das, Jhumki, Rawat, Amit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063417/
https://www.ncbi.nlm.nih.gov/pubmed/32181273
http://dx.doi.org/10.1016/j.gendis.2019.10.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063417/
https://www.ncbi.nlm.nih.gov/pubmed/32181273
http://dx.doi.org/10.1016/j.gendis.2019.10.002

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