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- W4386822729 abstract "Background: Mucopolysaccharidosis type III (MPS III) is the type of mucopolysaccharidosis that has fewer systemic signs and symptoms, however, it has the most severe neurological impairment. There are four types of MPS III, determined by the mutation in the gene responsible for the enzyme that becomes deficient in degrading intracellular glycosaminoglycan, which is responsible for the clinical picture." @default.
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- W4386822729 date "2023-09-01" @default.
- W4386822729 modified "2023-09-26" @default.
- W4386822729 title "Mucopolysaccharidosis III at the reference center for rare diseases of Ceará" @default.
- W4386822729 doi "https://doi.org/10.1055/s-0043-1774449" @default.
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