Monoaminergic control of spinal locomotor networks in SOD1(G93A) newborn mice

Mutations in the gene that encodes Cu/Zn-superoxide dismutase (SOD1) are the cause of approximately 20% of familial forms of amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disease characterized by the progressive loss of motor neurons. While ALS symptoms appear in adulthood, spinal m...

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Detalles Bibliográficos
Autores principales: Milan, Léa, Barrière, Grégory, De Deurwaerdère, Philippe, Cazalets, Jean-René, Bertrand, Sandrine S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081764/
https://www.ncbi.nlm.nih.gov/pubmed/25071458
http://dx.doi.org/10.3389/fncir.2014.00077

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081764/
https://www.ncbi.nlm.nih.gov/pubmed/25071458
http://dx.doi.org/10.3389/fncir.2014.00077

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