Common variable immunodeficiency associated with microdeletion of chromosome 1q42.1-q42.3 and inositol 1,4,5-trisphosphate kinase B (ITPKB) deficiency

Common variable immunodeficiency (CVID) is a heterogenous disorder characterized by hypogammaglobulinemia and impaired specific antibody response and increased susceptibility to infections, autoimmunity and malignancies. A number of gene mutations, including ICOS, TACI and BAFF-R, and CD19, CD20, CD...

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Detalles Bibliográficos
Autores principales: Louis, Ankmalika G, Yel, Leman, Cao, Jia N, Agrawal, Sudhanshu, Gupta, Sudhir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735063/
https://www.ncbi.nlm.nih.gov/pubmed/26900472
http://dx.doi.org/10.1038/cti.2015.41

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735063/
https://www.ncbi.nlm.nih.gov/pubmed/26900472
http://dx.doi.org/10.1038/cti.2015.41

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