Calcium is reduced in presynaptic mitochondria of motor nerve terminals during neurotransmission in SMA mice

Spinal muscular atrophy (SMA) is an autosomal recessive degenerative motor neuron disease characterized by symmetrical muscle weakness and atrophy of limb and trunk muscles being the most severe genetic disease in children. In SMA mouse models, motor nerve terminals display neurotransmitter release...

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Detalles Bibliográficos
Autores principales: Lopez-Manzaneda, Mario, Franco-Espin, Julio, Tejero, Rocio, Cano, Raquel, Tabares, Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
General Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127408/
https://www.ncbi.nlm.nih.gov/pubmed/33693569
http://dx.doi.org/10.1093/hmg/ddab065

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127408/
https://www.ncbi.nlm.nih.gov/pubmed/33693569
http://dx.doi.org/10.1093/hmg/ddab065

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