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Clinical profile and molecular characterization of Galactosemia in Brazil: identification of seven novel mutations
(BioMed Central, 2016)
Abstract
Background
Classical Galactosemia (CG) is an inborn error of galactose metabolism caused by the deficiency of the galactose-1-phosphate uridyltransferase enzyme. ...
Clinical Profile And Molecular Characterization Of Galactosemia In Brazil: Identification Of Seven Novel Mutations
(Biomed Central LtdLondon, 2016)
Clinical Profile And Molecular Characterization Of Galactosemia In Brazil: Identification Of Seven Novel Mutations
(BIOMED CENTRAL LTDLONDON, 2016)
Clinical profile and molecular characterization of Galactosemia in Brazil: identification of seven novel mutations
(2016-05-12)
Abstract
Background
Classical Galactosemia (CG) is an inborn error of galactose metabolism caused by the deficiency of the galactose-1-phosphate uridyltransferase enzyme. It ...