Monozygotic Twins Suffering From Sodium Taurocholate Cotransporting Polypeptide Deficiency: A Case Report
Author:
Funder
National Natural Science Foundation of China
Publisher
Frontiers Media SA
Subject
Pediatrics, Perinatology and Child Health
Reference22 articles.
1. Genetic polymorphisms in Na+-taurocholate co-transporting polypeptide (NTCP) and ileal apical sodium-dependent bile acid transporter (ASBT) and ethnic comparisons of functional variants of NTCP among Asian populations;Pan;Xenobiotica,2011
2. The sodium bile salt cotransport family SLC10;Hagenbuch;Pflugers Arch,2004
3. Sodium-dependent bile salt transporters of the SLC10A transporter family: more than solute transporters;Anwer;Pflugers Arch,2014
4. Sodium taurocholate cotransporting polypeptide deficiency manifesting as cholestatic jaundice in early infancy: a complicated case study;Song;Zhongguo Dang Dai Er Ke Za Zhi,2017
5. Molecular cloning, chromosomal localization, and functional characterization of a human liver Na+/bile acid cotransporter;Hagenbuch;J Clin Invest,1994
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1. NTCP Deficiency Affects the Levels of Circulating Bile Acids and Induces Osteoporosis;Frontiers in Endocrinology;2022-07-22
2. Hepatic Expression of the Na+-Taurocholate Cotransporting Polypeptide Is Independent from Genetic Variation;International Journal of Molecular Sciences;2022-07-05
3. Sodium taurocholate co-transporting polypeptide deficiency;Clinics and Research in Hepatology and Gastroenterology;2022-03
4. De novo mutation loci and clinical analysis in a child with sodium taurocholate cotransport polypeptide deficiency: A case report;World Journal of Clinical Cases;2021-12-26
5. Clinical characterization of NTCP deficiency in paediatric patients : A case‐control study based on SLC10A1 genotyping analysis;Liver International;2021-08-25
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