UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis.

Iolascon, A

UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis. [electronic resource] - Blood Feb 1998 - 1093 p. digital

Publication Type: Letter

0006-4971


Female
Glucuronosyltransferase--genetics
Humans
Infant, Newborn
Male
Polymorphism, Genetic
Promoter Regions, Genetic
Spherocytosis, Hereditary--genetics