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Sanfilippo syndrome: causes, consequences, and treatments

Sanfilippo syndrome, or mucopolysaccharidosis (MPS) type III, refers to one of five autosomal recessive, neurodegenerative lysosomal storage disorders (MPS IIIA to MPS IIIE) whose symptoms are caused by the deficiency of enzymes involved exclusively in heparan sulfate degradation. The primary charac...

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Detalles Bibliográficos
Autor principal:	Fedele, Anthony O
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove Medical Press 2015
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664539/ https://www.ncbi.nlm.nih.gov/pubmed/26648750 http://dx.doi.org/10.2147/TACG.S57672

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