LRBA in the endomembrane system

Bi-allelic mutations in LRBA (from Lipopolysaccharide-responsive and beige-like anchor protein) result in a primary immunodeficiency with clinical features ranging from hypogammaglobulinemia and lymphoproliferative syndrome to inflammatory bowel disease and heterogeneous autoimmune manifestations. L...

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Bibliografiske detaljer
Udgivet i:Colomb Med (Cali)
Main Authors: Martínez Jaramillo, Catalina, Trujillo-Vargas, Claudia M.
Format: Artigo
Sprog:Inglês
Udgivet: Universidad del Valle 2018
Fag:
Review Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6220489/
https://ncbi.nlm.nih.gov/pubmed/30410199
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.25100/cm.v49i2.3802
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