Primary bile acid malabsorption caused by mutations in the ileal sodium- dependent bile acid transporter gene (SLC10A2)

Journal of Clinical Investigation

Volumn 99, Issue 8, 1997, Pages 1880-1887

  Oelkers, Peter ^a,c   Kirby, Lyndon C ^a,d   Heubi, James E ^b   Dawson, Paul A ^a  

^a WAKE FOREST SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF CINCINNATI   (United States)

^c Och Spine at New York Presbyterian Hospitals   (United States)

^d EAST CAROLINA UNIVERSITY   (United States)

Author keywords

bile acid malabsorption; bile salts; cholesterol; genetic disease; mutation analysis

Indexed keywords

BILE ACID; BILE SALT; CARRIER PROTEIN; CHOLESTEROL; GENE PRODUCT; SODIUM ION;

ALLELE; ANIMAL CELL; ARTICLE; BILE ACID SYNTHESIS; CHOLESTEROL BLOOD LEVEL; CONTROLLED STUDY; DIARRHEA; ENTEROHEPATIC CIRCULATION; GENE MUTATION; GENETIC POLYMORPHISM; HUMAN; ILEUM; MALABSORPTION; MOLECULAR CLONING; MONKEY; NONHUMAN; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; STEATORRHEA;

EID: 0030944084     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI119355     Document Type: Article

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