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    A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome

    Mucopolysaccharidosis II (MPS II, Hunter syndrome; OMIM 309900) is an X-linked lysosomal storage disease caused by a deficiency in the enzyme iduronate-2-sulfatase (IDS), leading to accumulation of glycosamino...

    Yo Kyung Chung, Young Bae Sohn, Jong Mun Sohn, Jieun Lee… in Glycoconjugate Journal (2014)