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Published in 2020 at "Metabolic Brain Disease"
DOI: 10.1007/s11011-020-00592-5
Abstract: Hunter syndrome or mucopolysaccharidosis type II (MPS II) is an X-linked recessive disease caused by the deficiency of iduronate 2-sulfatase (IDS), leading to storage of undegraded heparan and dermatan sulfate. Patients with the severe form…
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Keywords:
mucopolysaccharidosis type;
brain;
activation;
evidence inflammasome ... See more keywords