Mitochondrial Dysfunction in Spinal Muscular Atrophy

Spinal muscular atrophy (SMA) is a devastating neuromuscular disorder caused by recessive mutations in the SMN1 gene, globally affecting ~8–14 newborns per 100,000. The severity of the disease depends on the residual levels of functional survival of motor neuron protein, SMN. SMN is a ubiquitously e...

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Detalles Bibliográficos
Autores principales: Zilio, Eleonora, Piano, Valentina, Wirth, Brunhilde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503857/
https://www.ncbi.nlm.nih.gov/pubmed/36142791
http://dx.doi.org/10.3390/ijms231810878

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503857/
https://www.ncbi.nlm.nih.gov/pubmed/36142791
http://dx.doi.org/10.3390/ijms231810878

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