Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan...
Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan from 1995-2012
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England: BioMed Central Ltd
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English
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England: BioMed Central Ltd
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Mucopolysaccharidosis type II (MPS II) is an X-linked recessive, multisystemic lysosomal storage disorder caused by a deficiency of iduronate-2-sulfatase. MPS II has a variable age of onset and variable rate of progression. In Asian countries, there is a relatively higher incidence of MPS II compared to other types of MPS.
A retrospective analys...
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Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan from 1995-2012
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4924312
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4924312
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ISSN
1750-1172
E-ISSN
1750-1172
DOI
10.1186/s13023-016-0471-6