[Roles of UGT 1A1 gene mutation in the development of neonatal hyperbilirubinemia in Guangxi].

Zhonghua er ke za zhi. Chinese journal of pediatrics

Volumn 48, Issue 9, 2010, Pages 646-649

  Gao, Zong yan ^a   Zhong, Dan ni ^b   Liu, Y ^b   Liu, You nan ^b   Wei, Lu ming ^b  

^a GUANGXI MEDICAL UNIVERSITY   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN URIDINE DIPHOSPHOGLUCURONOSYL TRANSFERASE 1A1; BILIRUBIN URIDINE-DIPHOSPHOGLUCURONOSYL TRANSFERASE 1A1; GLUCURONOSYLTRANSFERASE;

ARTICLE; CASE CONTROL STUDY; CHINA; GENETICS; GENOTYPE; HUMAN; MUTATION; NEWBORN; NEWBORN JAUNDICE;

CASE-CONTROL STUDIES; CHINA; GENOTYPE; GLUCURONOSYLTRANSFERASE; HUMANS; HYPERBILIRUBINEMIA, NEONATAL; INFANT, NEWBORN; MUTATION;

EID: 79958071365     PISSN: 05781310     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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