The genetic basis of Gilbert's syndrome

Lancet

Volumn 347, Issue 9001, 1996, Pages 557-558

  Sato, H ^a   Adachi, Y ^a   Koiwai, O ^a  

^a SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; GLUCURONIC ACID; GLUCURONOSYLTRANSFERASE; LIVER ENZYME;

ADOLESCENT; ADULT; BILIRUBIN BLOOD LEVEL; CLINICAL ARTICLE; CRIGLER NAJJAR SYNDROME; ENZYME ACTIVITY; GENE MUTATION; GENETIC ANALYSIS; GENETIC TRANSCRIPTION; GILBERT DISEASE; HUMAN; NOTE; PRIORITY JOURNAL; TATA BOX;

EID: 0030053274     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(96)91266-0     Document Type: Article

References (5)

1. Pj Bosma Rj Chowdhury C. Bakker The genetic basis of the reduced expression of bilirubin UDP-glucuronosyl-transferase 1 in Gilbert's syndrome N Engl J Med 333 1995 1171 1175
2. S. Aono Y. Adachi E. Uyama Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome Lancet 345 1995 958 959
3. O. Koiwai M. Nishizawa K. Hasada Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase Hum Mol Genet 4 1995 1183 1186
4. Y. Soeda K. Yamamoto Y. Adachi Predicted homozygous mis-sense mutation in Gilbert's syndrome Lancet 346 1995 1494
5. R. Schmid Gilbert's syndrome: a legitimate genetic anomaly? N Engl J Med 333 1995 1217 1218