Revisiting the role of mitochondria in spinal muscular atrophy

Spinal muscular atrophy (SMA) is an autosomal recessive motor neuron disease of variable clinical severity that is caused by mutations in the survival motor neuron 1 (SMN1) gene. Despite its name, SMN is a ubiquitous protein that functions within and outside the nervous system and has multiple cellu...

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Detalles Bibliográficos
Autores principales: James, Rachel, Chaytow, Helena, Ledahawsky, Leire M., Gillingwater, Thomas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195803/
https://www.ncbi.nlm.nih.gov/pubmed/33821292
http://dx.doi.org/10.1007/s00018-021-03819-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195803/
https://www.ncbi.nlm.nih.gov/pubmed/33821292
http://dx.doi.org/10.1007/s00018-021-03819-5

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