Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: A common missense mutation among Japanese, Koreans and Chinese

Biochemistry and Molecular Biology International

Volumn 46, Issue 1, 1998, Pages 21-26

  Akaba, Kazuhiro ^a   Kimura, Toshiyuki ^a   Sasaki, Ayako ^a   Tanabe, Saori ^a   Ikegami, Tohru ^a   Hashimoto, Motoya ^b   Umeda, Hitoshi ^c   Yoshida, Hiroshi ^d   Umetsu, Kazuo ^a   Chiba, Hitoshi ^e   Yuasa, Isao ^f   Hayasaka, Kiyoshi ^a  

^a YAMAGATA UNIVERSITY   (Japan)

^b Saiseikai Yamagata Saisei Hospital   (Japan)

^c Yamagata Prefectural Nihonkai Hospital   (Japan)

^d Shounai Hospital   (Japan)

^e HOKKAIDO UNIVERSITY   (Japan)

^f TOTTORI UNIVERSITY   (Japan)

Author keywords

Bilirubin uridine diphosphate glucuronosyltransferase; Hyperbilirubinemia

Indexed keywords

BILIRUBIN; GLUCURONOSYLTRANSFERASE;

AMINO ACID SUBSTITUTION; ARTICLE; CHINA; CLINICAL ARTICLE; CONTROLLED STUDY; ETHNIC GROUP; GENE FREQUENCY; HETEROZYGOTE; HOMOZYGOTE; HUMAN; HUMAN CELL; JAPAN; KOREA; MISSENSE MUTATION; NEWBORN; NEWBORN JAUNDICE;

EID: 0031719562     PISSN: 10399712     EISSN: None     Source Type: Journal    
DOI: 10.1080/15216549800203512     Document Type: Article

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