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Introduccion. La enfermedad de Hunter es un trastorno lisosomico caracterizado por la deficiencia de la enzima iduronato-2-sulfato sulfatasa (IDS) (EC 3.1.6.13). Esta enfermedad, al igual que muchosContinue Reading
INTRODUCTION Hunter syndrome is a lysosomal disorder characterized by iduronate 2-sulphate sulphatase (IDS) genetic deficiency. Although MPS type II (Hunter) has no cure, enzyme replacement therapyContinue Reading