NTCP deficiency: A new inherited disease of bile acid transport

Clinics and Research in Hepatology and Gastroenterology

Volumn 39, Issue 1, 2015, Pages 7-8

  Erlinger, Serge ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; BILE ACID; HISTIDINE; SODIUM BILE ACID COTRANSPORTER; TAUROCHOLIC ACID; CHOLIC ACID DERIVATIVE; COTRANSPORTER; ORGANIC ANION TRANSPORTER;

AMINO ACID SUBSTITUTION; ARTICLE; BILE ACID BLOOD LEVEL; BILIARY TRACT DISEASE; CHOLESTASIS; GENE SEQUENCE; GENETIC CODE; INHERITANCE; LIVER FUNCTION TEST; NTCP DEFICIENCY; POINT MUTATION; PROTEIN DEFICIENCY; PRURITUS; BLOOD; DEFICIENCY; FEMALE; GENETICS; HUMAN; INBORN ERROR OF STEROID METABOLISM;

CHOLIC ACIDS; FEMALE; HUMANS; ORGANIC ANION TRANSPORTERS, SODIUM-DEPENDENT; STEROID METABOLISM, INBORN ERRORS; SYMPORTERS;

EID: 84922185017     PISSN: 22107401     EISSN: 2210741X     Source Type: Journal    
DOI: 10.1016/j.clinre.2014.07.011     Document Type: Article

References (9)

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