Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11

OBJECTIVE: Hereditary spastic paraplegias (HSPs) are among the most genetically diverse inherited neurological disorders, with over 70 disease loci identified (SPG1-71) to date. SPG15 and SPG11 are clinically similar, autosomal recessive disorders characterized by progressive spastic paraplegia alon...

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Detalles Bibliográficos
Autores principales: Renvoisé, Benoît, Chang, Jaerak, Singh, Rajat, Yonekawa, Sayuri, FitzGibbon, Edmond J, Mankodi, Ami, Vanderver, Adeline, Schindler, Alice B, Toro, Camilo, Gahl, William A, Mahuran, Don J, Blackstone, Craig, Pierson, Tyler Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078876/
https://www.ncbi.nlm.nih.gov/pubmed/24999486
http://dx.doi.org/10.1002/acn3.64

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078876/
https://www.ncbi.nlm.nih.gov/pubmed/24999486
http://dx.doi.org/10.1002/acn3.64

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