Analysis of uridine diphosphate glucuronosyl transferase 1A1 gene mutations in neonates with unconjugated hyperbilirubinemia.

Guo, X H

Analysis of uridine diphosphate glucuronosyl transferase 1A1 gene mutations in neonates with unconjugated hyperbilirubinemia. [electronic resource] - Genetics and molecular research : GMR May 2016

Publication Type: Journal Article

1676-5680

10.4238/gmr.15028373 doi


Bilirubin--blood
Female
Gene Frequency
Genetic Association Studies
Genetic Predisposition to Disease
Genotype
Glucuronosyltransferase--genetics
Heterozygote
Homozygote
Humans
Hyperbilirubinemia, Hereditary--blood
Infant, Newborn
Male
Mutation
Polymorphism, Single Nucleotide