Rocha, Susana <br/><br/>
Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region--a comparison of the bilirubin plasmatic levels in the different clinical forms.  [electronic resource] 

 -  Blood cells, molecules & diseases   
 - 117-9 p.  digital 
<br/><br/> Publication Type: Comparative Study; Letter 
<br/><br/><label>ISSN: </label>1096-0961 
<br/><br/><label>Standard No.: </label>10.1016/j.bcmd.2009.10.012  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Bilirubin--blood<br/>Gilbert Disease--complications<br/>Glucuronosyltransferase--genetics<br/>Humans<br/>Polymorphism, Genetic<br/>Prognosis<br/>Promoter Regions, Genetic<br/>Spherocytosis, Hereditary--complications