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Data from: Assessment of dysmyelination with RAFFn MRI: application to murine MPS I
- 负责人:
- DOI:
- doi:10.5061/dryad.ng64q
- 摘要:
- Type I mucopolysaccharidosis (MPS I) is an autosomal recessive lysosomal storage disorder with neurological features. Humans and laboratory animals
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