Familial NTCPD Presenting with Persistent Hypercholanemia and Co-Existing with a Series of Novel Heterozygous Mutations
Clinics and research in hepatology and gastroenterology（2024）
Key words
Sodium taurocholate cotransporter polypeptide deficiency,SLC10A1 gene,Persistent hypercholanemia,Transient cholestatic hepatitis
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