Motor Neuron Gene Therapy: Lessons from Spinal Muscular Atrophy for Amyotrophic Lateral Sclerosis

Spinal muscular atrophy (SMA) and amyotrophic lateral sclerosis (ALS) are severe nervous system diseases characterized by the degeneration of lower motor neurons. They share a number of additional pathological, cellular, and genetic parallels suggesting that mechanistic and clinical insights into on...

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Detalles Bibliográficos
Autores principales: Tosolini, Andrew P., Sleigh, James N.
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/PMC5725447/
https://www.ncbi.nlm.nih.gov/pubmed/29270111
http://dx.doi.org/10.3389/fnmol.2017.00405

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725447/
https://www.ncbi.nlm.nih.gov/pubmed/29270111
http://dx.doi.org/10.3389/fnmol.2017.00405

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