Mechanisms of inherited deficiencies of multiple UDP- glucuronosyltransferase isoforms in two patients with Crigler-Najjar syndrome, type I

FASEB Journal

Volumn 6, Issue 10, 1992, Pages 2859-2863

  Bosma, P J ^a   Chowdhury, J R ^a   Huang, T J ^a   Lahiri, P ^a   Elferink, R P J O ^a   Van Es, H H G ^a   Lederstein, M ^a   Whitington, P F ^a   Jansen, P L M ^a   Chowdhury, N R ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

4 nitrophenol; bilirubin; Crigler Najjar syndrome; exon skipping; multiple isoform deficiency; sequence abnormality; type I; UDP glucuronosyltransferase

Indexed keywords

BILIRUBIN; GLUCURONOSYLTRANSFERASE; ISOENZYME; MESSENGER RNA;

AMINO ACID SUBSTITUTION; ARTICLE; BILIRUBIN METABOLISM; CASE REPORT; CRIGLER NAJJAR SYNDROME; ENZYME ACTIVITY; ENZYME STRUCTURE; EXON; HUMAN; HUMAN TISSUE; PRIORITY JOURNAL;

EID: 0026668559     PISSN: 08926638     EISSN: None     Source Type: Journal    
DOI: 10.1096/fasebj.6.10.1634050     Document Type: Article

References (0)