Strumpellin and Spartin, Hereditary Spastic Paraplegia Proteins, are Binding Partners

Hereditary spastic paraplegia (HSP) is one of the most heterogeneous neurodegenerative diseases with more than 50 identified genes causing a relatively stereotypical phenotypic presentation. Recent studies of HSP pathogenesis have suggested the existence of shared biochemical pathways that are cruci...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Jiali, Hedera, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2015
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426939/
https://www.ncbi.nlm.nih.gov/pubmed/25987849
http://dx.doi.org/10.4137/JEN.S22969

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426939/
https://www.ncbi.nlm.nih.gov/pubmed/25987849
http://dx.doi.org/10.4137/JEN.S22969

Ejemplares similares