The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
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1. A novel ABCB11 variant in compound heterozygosity: BRIC2 or PFIC2?;Gastroenterology Report;2023-12-22
2. Genetic alterations and molecular mechanisms underlying hereditary intrahepatic cholestasis;Frontiers in Pharmacology;2023-05-31
3. A study of exons 14, 15, and 24 of the ABCB11 gene in Egyptian children with normal GGT cholestasis;Arab Journal of Gastroenterology;2022-02
4. ATP8B1, ABCB11, and ABCB4 Genes Defects: Novel Mutations Associated with Cholestasis with Different Phenotypes and Outcomes;The Journal of Pediatrics;2021-09
5. ABCB11 deficiency presenting as transient neonatal cholestasis: Correlation with genotypes and BSEP expression;Liver International;2020-10-13
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