Microglial Activation in the Pathogenesis of Huntington’s Disease

Huntington’s disease (HD) is an autosomal dominantly inherited neurodegenerative disorder caused by expanded CAG trinucleotide repeats (>36) in exon 1 of HTT gene that encodes huntingtin protein. Although HD is characterized by a predominant loss of neurons in the striatum and cortex, previous st...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Hui-Ming, Yang, Su, Huang, Shan-Shan, Tang, Bei-Sha, Guo, Ji-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474461/
https://www.ncbi.nlm.nih.gov/pubmed/28674491
http://dx.doi.org/10.3389/fnagi.2017.00193

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474461/
https://www.ncbi.nlm.nih.gov/pubmed/28674491
http://dx.doi.org/10.3389/fnagi.2017.00193

Ejemplares similares