Found: 4
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Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort.
- Published in:
- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1750-1172-9-18
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- Publication type:
- Article
Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort.
- Published in:
- 2014
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- Publication type:
- journal article
NPC1: Complete genomic sequence, mutation analysis, and characterization of haplotypes.
- Published in:
- Human Mutation, 2002, v. 19, n. 1, p. 30, doi. 10.1002/humu.10016
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- Publication type:
- Article
Enzymatic characterization of novel arylsulfatase A variants using human arylsulfatase A-deficient immortalized mesenchymal stromal cells.
- Published in:
- Human Mutation, 2017, v. 38, n. 11, p. 1511, doi. 10.1002/humu.23306
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- Publication type:
- Article