JAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference17 articles.
1. Alagille syndrome: pathogenesis, diagnosis and management;PD Turnpenny;Eur J Hum Genet: EJHG,2012
2. Studies of the aetiology of neonatal hepatitis and biliary atresia;DM Danks;Arch Dis Child,1977
3. Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases;D Alagille;J Pediatr,1987
4. Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families;ID Krantz;Am J Hum Genet,1998
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