Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency.

Kaplan, M

Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency. [electronic resource] - Journal of perinatology : official journal of the California Perinatal Association Dec 2001 - S30-4; discussion S35-9 p. digital

Publication Type: Journal Article

0743-8346

10.1038/sj.jp.7210630 doi


Bilirubin--metabolism
Gilbert Disease--complications
Glucuronosyltransferase--metabolism
Glycogen Storage Disease Type I--complications
Hemolysis
Humans
Infant, Newborn
Jaundice, Neonatal--etiology
Liver--metabolism
Promoter Regions, Genetic