Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients

Journal of Maternal-Fetal and Neonatal Medicine

Volumn 24, Issue 2, 2011, Pages 313-316

  Narter, Fatma ^a   Can, Gülay ^a   Ergen, Arzu ^b   Isbir, Turgay ^b   Ince, Zeynep ^a   Çoban, Asuman ^a  

^a ISTANBUL UNIVERSITY   (Turkey)

^b ISTANBUL UNIVERSITY   (Turkey)

Author keywords

G71R mutation; Neonatal hyperbilirubinemia; UGT1A1 gene

Indexed keywords

ARGININE; BILIRUBIN; GLUCURONOSYLTRANSFERASE 1A1; GLYCINE;

AGAR GEL ELECTROPHORESIS; ARTICLE; BILIRUBIN BLOOD LEVEL; CHILD HEALTH; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; DISEASE SEVERITY; FEMALE; GENE FREQUENCY; GENE LOCATION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; HUMAN; MALE; MUTATION RATE; MUTATIONAL ANALYSIS; NEWBORN; NEWBORN JAUNDICE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; TURKEY (REPUBLIC);

AMINO ACID SUBSTITUTION; ARGININE; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; GESTATIONAL AGE; GLUCURONOSYLTRANSFERASE; GLYCINE; HUMANS; HYPERBILIRUBINEMIA, NEONATAL; INFANT, NEWBORN; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; TURKEY;

EID: 78651427828     PISSN: 14767058     EISSN: 14764954     Source Type: Journal    
DOI: 10.3109/14767058.2010.490889     Document Type: Article

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