Magnetic resonance reveals mitochondrial dysfunction and muscle remodelling in spinal muscular atrophy

Genetic therapy has changed the prognosis of hereditary proximal spinal muscular atrophy, although treatment efficacy has been variable. There is a clear need for deeper understanding of underlying causes of muscle weakness and exercise intolerance in patients with this disease to further optimize t...

Descripción completa

Detalles Bibliográficos
Autores principales: Habets, Laura E, Bartels, Bart, Asselman, Fay-Lynn, Hooijmans, Melissa T, van den Berg, Sandra, Nederveen, Aart J, van der Pol, W Ludo, Jeneson, Jeroen A L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9128825/
https://www.ncbi.nlm.nih.gov/pubmed/34788410
http://dx.doi.org/10.1093/brain/awab411

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9128825/
https://www.ncbi.nlm.nih.gov/pubmed/34788410
http://dx.doi.org/10.1093/brain/awab411

Ejemplares similares