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Published in 2018 at "Molecular genetics and metabolism"
DOI: 10.1016/j.ymgme.2018.07.013
Abstract: Mucopolysaccharidosis type II (MPS II or Hunter syndrome) is a lysosomal storage disorder caused by a deficiency of iduronate-2-sulfatase (IDS), an enzyme that catabolizes glycosaminoglycans (GAGs) including heparan sulfate (HS) and dermatan sulfate (DS). GAG…
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Keywords:
gag accumulation;
mucopolysaccharidosis type;
sulfate;
heparan sulfate ... See more keywords