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    • Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type ii (hunter syndrome) 

      Silva, Edina Mariko Koga da [UNIFESP]; Strufaldi, Maria Wany Louzada [UNIFESP]; Andriolo, Regis Bruni; Silva, Laercio Antonio da [UNIFESP] (Wiley, 2016)
      Background Mucopolysaccharidosis II, also known as Hunter syndrome, is a rare, X-linked disease caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase, which catalyses a step in the catabolism of glycosaminoglycans. ...