A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis

Nature Genetics

Volumn 18, Issue 3, 1998, Pages 219-224

  Bull, Laura N ^a   Van Eijk, Michiel J T ^b   Pawlikowska, Ludmila ^a,c   DeYoung, Joseph A ^a   Juijn, Jenneke A ^b   Liao, Mira ^a   Klomp, Leo W J ^b   Lomri, Noureddine ^d   Berger, Ruud ^b   Scharschmidt, Bruce F ^d,e   Knisely, Alexander S ^f   Houwen, Roderick H J ^b   Freimer, Nelson B ^a,c  

^a Dept of Psychiatry Und Liver Center ^*  (United States)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e NOVARTIS PHARMA AG   (Switzerland)

^f Unipath   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ADENOSINE TRIPHOSPHATASE; AMINOPHOSPHOLIPID; BILE ACID; COMPLEMENTARY DNA;

AMINO ACID SEQUENCE; ARTICLE; CHROMOSOME 18Q; CONTROLLED STUDY; ENTEROHEPATIC CIRCULATION; GENE EXPRESSION; GENE MUTATION; GENETIC DISORDER; HAPLOTYPE; HUMAN; INTRAHEPATIC CHOLESTASIS; PHOSPHOLIPID TRANSFER; PRIORITY JOURNAL; SMALL INTESTINE;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; BLOTTING, NORTHERN; CHOLESTASIS; CHOLESTASIS, INTRAHEPATIC; CHROMOSOME MAPPING; EUROPE; FEMALE; HOMOZYGOTE; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; SEQUENCE DELETION; UNITED STATES;

EID: 0031907132     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0398-219     Document Type: Article

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