A case of anorexia nervosa with hyperbilirubinaemia in a patient homozygous for a mutation in the bilirubin UDP-glucuronosyltransferase gene

European Journal of Pediatrics

Volumn 158, Issue 7, 1999, Pages 547-549

  Maruo, Y ^a   Wada, S ^a   Yamamoto, K ^a   Sato, H ^a   Yamano, T ^a   Shimada, M ^a  

^a SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

Author keywords

Anorexia nervosa; Bilirubin UDP glucuronosyltransferase gene; Gilbert syndrome; Homozygous missense mutation; UGT1 A1

Indexed keywords

GLUCURONOSYLTRANSFERASE;

ANOREXIA NERVOSA; ARTICLE; CASE REPORT; CHILD; FEMALE; GENE MUTATION; GILBERT DISEASE; HOMOZYGOSITY; HUMAN; HYPERBILIRUBINEMIA; MISSENSE MUTATION; PRIORITY JOURNAL; SCHOOL CHILD;

ANOREXIA NERVOSA; BILIRUBIN; CHILD; FEMALE; GILBERT DISEASE; GLUCURONOSYLTRANSFERASE; HUMANS; SENSITIVITY AND SPECIFICITY;

EID: 0033000014     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310051143     Document Type: Article

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