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...

Descripción completa

Detalles Bibliográficos
Autores principales: Garbuzova-Davis, Svitlana, Mirtyl, Santhia, Sallot, Sebastian A, Hernandez-Ontiveros, Diana G, Haller, Edward, Sanberg, Paul R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835134/
https://www.ncbi.nlm.nih.gov/pubmed/24225396
http://dx.doi.org/10.1186/1471-2377-13-174

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835134/
https://www.ncbi.nlm.nih.gov/pubmed/24225396
http://dx.doi.org/10.1186/1471-2377-13-174

Ejemplares similares