Screening for G71R mutation of the UDP-glucuronosyltransferase 1 (UGT1A1) gene in neonates with pathologic and prolonged hyperbilirubinemia in Turkey

International Journal of Clinical Pharmacology and Therapeutics

Volumn 48, Issue 8, 2010, Pages 504-508

  Kilic, I ^a   Koseler, A ^a   Cakaloz, I ^a   Atalay, E ^a  

^a PAMUKKALE UNIVERSITY   (Turkey)

Author keywords

G R mutation; Pathologic hyperbilirubinemia; Prolonged hyperbilirubinemia; Turkish population; UGT1A1 gene

Indexed keywords

BILIRUBIN; GLUCURONOSYLTRANSFERASE 1A1;

ALLELE; ARTICLE; BILIRUBIN BLOOD LEVEL; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC SCREENING; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; NEWBORN; NEWBORN JAUNDICE; TURKEY (REPUBLIC);

EID: 77955672112     PISSN: 09461965     EISSN: None     Source Type: Journal    
DOI: 10.5414/CPP48504     Document Type: Article

References (20)

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