Murine LRBA deficiency causes CTLA‐4 deficiency in Tregs without progression to immune dysregulation
Author:
Affiliation:
1. Immunology Division, Garvan Institute for Medical Research Sydney NSW Australia
2. John Curtin School of Medical Research, Australian National University Canberra ACT Australia
Funder
National Health and Medical Research Council
National Institutes of Health
Publisher
Wiley
Subject
Cell Biology,Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1038/icb.2017.50
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3. Identification of a Novel Lipopolysaccharide-Inducible Gene with Key Features of Both a Kinase Anchor Proteins and chs1/beige Proteins
4. Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity
5. LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency
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