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References OMIM Gene GeneReviews HGMD HGNC
last update : 19/09/2006
Symbol GPX1
Location 3p21.2
Name hemolytic anemia
Corresponding gene GPX1
Main clinical features hemolytic disease of the newborn with hyperbilirubinemia and Heinz bodies, associated with partial deficiency of red cell glutathione peroxidase
Genetic determination autosomal dominant
Function/system disorder hematology
Type disease
Gene product
Name glutathione peroxidase 1, cellular (GPX1)