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Blood-brain barrier impairment in MPS III patients
BACKGROUND: Mucopolysaccharidosis type III (MPS III) is an autosomal recessive disorder caused by deficiency of a specific enzyme leading to heparan sulfate (HS) accumulation within cells and to eventual progressive cerebral and systemic organ abnormalities. Different enzyme deficiencies comprise th...
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| Main Authors: | , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2013
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3835134/ https://ncbi.nlm.nih.gov/pubmed/24225396 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-13-174 |
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