Associated Papers
Alagille Syndrome: Unraveling the Complexities of Genotype-Phenotype Relationships and Exploring Avenues for Improved Diagnosis and Treatment.
Sharma P et al.
Cell Biology International, 2025
Novel JAG1 variants leading to Alagille syndrome in two Chinese cases.
Feng X et al.
Scientific Reports, 2024
38245625 (PubMed )
Supplement: 41598_2024_52357_MOESM1_ESM.xlsx › Sheet1
Previously Undescribed Family Mutation in the JAG1 Gene as a Cause for Alagille Syndrome.
Muñoz-Aguilar G et al.
Journal of Pediatric Gastroenterology and Nutrition, 2017
GATA6 Mutation: A Rare Genetic Cause of Hepatobiliary Disease.
Ferreira S et al.
Journal of Pediatric Gastroenterology and Nutrition, 2017
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