Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase

Human Molecular Genetics

Volumn 4, Issue 7, 1995, Pages 1183-1186

  Koiwai, Osamu ^a   Nishizawa, Miwako ^a   Hasada, Kayo ^a,b   Aono, Sachiko ^a,c   Adachi, Yukihiko ^a,d   Mamlya, Naoto ^a,e   Sato, Hiroshi ^a,f  

^a Laboratory of Biochemistry   (Japan)

^b AICHI CANCER CENTER HOSPITAL   (Japan)

^c INSTITUTE FOR DEVELOPMENTAL RESEARCH   (Japan)

^d KINKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^e NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^f SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; GLUCURONOSYLTRANSFERASE;

ADOLESCENT; ADULT; ANIMAL CELL; ARTICLE; BILIRUBIN METABOLISM; CLONING VECTOR; CONTROLLED STUDY; FEMALE; GENE MUTATION; GILBERT DISEASE; HETEROZYGOSITY; HUMAN; HUMAN TISSUE; HYPERBILIRUBINEMIA; MALE; NONHUMAN; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; ALLELES; AMINO ACID SEQUENCE; ANIMAL; BASE COMPOSITION; BASE SEQUENCE; BLOTTING, NORTHERN; CELL LINE; CHILD; DNA; EXONS; FEMALE; GENE EXPRESSION; GILBERT DISEASE; GLUCURONOSYLTRANSFERASE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; LIVER; MALE; MIDDLE AGE; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; RNA, MESSENGER; TRANSFECTION;

EID: 0029015847     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/4.7.1183     Document Type: Article

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