Abstracts from the Immunodeficiency Canada—7th SCID Symposium, Montreal, QC, 24 October 2019
Author:
Publisher
LymphoSign Journal Limited Partnership
Subject
General Earth and Planetary Sciences,General Environmental Science
Link
http://lymphosign.com/doi/pdf/10.14785/lymphosign-2019-0015
Reference65 articles.
1. LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency
2. Spectrum of Phenotypes Associated with Mutations in LRBA
3. Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study
4. Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked–like disorder caused by loss-of-function mutations in LRBA
5. A novel LPS-responsive beige-like anchor protein (LRBA) mutation presents with normal cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and overactive TH17 immunity
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