Clinical manifestations associated with novel mutations in the coiled-coil domain of STAT1
Author:
Affiliation:
1. Department of Pediatrics A Soroka, University Medical Center, Ben Gurion University of The Negev, Beer Sheva, Israel
2. Pediatric Allergy and Immunology Unit, E. Wolfson Medical Center, Holon and Tel-Aviv University, Tel-Aviv, Israel.
Abstract
Publisher
LymphoSign Journal Limited Partnership
Subject
General Earth and Planetary Sciences,General Environmental Science
Link
http://lymphosign.com/doi/pdf/10.14785/lpsn-2014-0021
Reference15 articles.
1. Inborn errors of human STAT1: allelic heterogeneity governs the diversity of immunological and infectious phenotypes
2. Crystal Structure of a Tyrosine Phosphorylated STAT-1 Dimer Bound to DNA
3. Impaired response to interferon-α/β and lethal viral disease in human STAT1 deficiency
4. Cerebral vasculitis associated with chronic mucocutaneous candidiasis
5. Enhancement of formation of the esophageal carcinogen benzylmethylnitrosamine from its precursors by Candida albicans
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