Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region--a comparison of the bilirubin plasmatic levels in the different clinical forms.

Authors	Susana Rocha, Elísio Costa, Fátima Ferreira, Esmeralda Cleto, José Barbot, Petronila Rocha-Pereira, Alexandre Quintanilha, Luís Belo, Alice Santos-Silva
Journal	Blood cells, molecules & diseases (Blood Cells Mol Dis) 2010 Mar-Apr Vol. 44 Issue 2 Pg. 117-9 ISSN: 1096-0961 [Electronic] United States
PMID	19931474 (Publication Type: Comparative Study, Letter)
Chemical References	UGT1A1 enzyme Glucuronosyltransferase Bilirubin
Topics	Bilirubin (blood) Gilbert Disease (complications, genetics) Glucuronosyltransferase (genetics) Humans Polymorphism, Genetic Prognosis Promoter Regions, Genetic Spherocytosis, Hereditary (complications, diagnosis, genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.

Realize the full power of the drug-disease research graph!