000 01413 a2200385 4500
005 20250515194736.0
264 0 _c20100413
008 201004s 0 0 eng d
022 _a1096-0961
024 7 _a10.1016/j.bcmd.2009.10.012
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRocha, Susana
245 0 0 _aHereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region--a comparison of the bilirubin plasmatic levels in the different clinical forms.
_h[electronic resource]
260 _bBlood cells, molecules & diseases
_c
300 _a117-9 p.
_bdigital
500 _aPublication Type: Comparative Study; Letter
650 0 4 _aBilirubin
_xblood
650 0 4 _aGilbert Disease
_xcomplications
650 0 4 _aGlucuronosyltransferase
_xgenetics
650 0 4 _aHumans
650 0 4 _aPolymorphism, Genetic
650 0 4 _aPrognosis
650 0 4 _aPromoter Regions, Genetic
650 0 4 _aSpherocytosis, Hereditary
_xcomplications
700 1 _aCosta, Elísio
700 1 _aFerreira, Fátima
700 1 _aCleto, Esmeralda
700 1 _aBarbot, José
700 1 _aRocha-Pereira, Petronila
700 1 _aQuintanilha, Alexandre
700 1 _aBelo, Luís
700 1 _aSantos-Silva, Alice
773 0 _tBlood cells, molecules & diseases
_gvol. 44
_gno. 2
_gp. 117-9
856 4 0 _uhttps://doi.org/10.1016/j.bcmd.2009.10.012
_zAvailable from publisher's website
999 _c19316241
_d19316241