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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...
Autores principales: | Morello, Giovanna, Spampinato, Antonio Gianmaria, Cavallaro, Sebastiano |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
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 |
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