Molecular Taxonomy of Sporadic Amyotrophic Lateral Sclerosis Using Disease-Associated Genes

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by selective loss of upper and lower motor neurons. Despite intensive research, the origin and progression of ALS remain largely unknown, suggesting that the traditional clinical diagnosis and treatment strategies...

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Detalles Bibliográficos
Autores principales: Morello, Giovanna, Spampinato, Antonio Gianmaria, Cavallaro, Sebastiano
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/PMC5395696/
https://www.ncbi.nlm.nih.gov/pubmed/28469596
http://dx.doi.org/10.3389/fneur.2017.00152

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395696/
https://www.ncbi.nlm.nih.gov/pubmed/28469596
http://dx.doi.org/10.3389/fneur.2017.00152

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