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Hepatology

Volumn 32, Issue 4 I, 2000, Pages 792-795

Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects

(5) Borlak, Jürgen a Thum, Thomas a Landt, Olfert b Erb, Katharina c Hermann, Robert c

a FRAUNHOFER INSTITUTE FOR TOXICOLOGY AND EXPERIMENTAL MEDICINE (Germany)

b TIB MOLBIOL (Germany)

c ASTA MEDICA AG (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; GLUCURONOSYLTRANSFERASE;

ALLELE; ARTICLE; BILIRUBIN BINDING; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; FLUORESCENCE; GENE MUTATION; GENOTYPE; GILBERT DISEASE; HUMAN; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TATA BOX;

EID: 0033802568 PISSN: 02709139 EISSN: None Source Type: Journal
DOI: 10.1053/jhep.2000.18193 Document Type: Article

Times cited : (84)

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