Resistance Exercise Training Rescues Mitochondrial Dysfunction in Skeletal Muscle of Patients with Myotonic Dystrophy Type 1

BACKGROUND: Myotonic dystrophy type 1 (DM1) is a dominant autosomal neuromuscular disorder caused by the inheritance of a CTG triplet repeat expansion in the Dystrophia Myotonica Protein Kinase (DMPK) gene. At present, no cure currently exists for DM1 disease. OBJECTIVE: This study investigates the...

Descripción completa

Detalles Bibliográficos
Autores principales: Di Leo, Valeria, Lawless, Conor, Roussel, Marie-Pier, Gomes, Tiago B., Gorman, Gráinne S., Russell, Oliver M., Tuppen, Helen A.L., Duchesne, Elise, Vincent, Amy E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657683/
https://www.ncbi.nlm.nih.gov/pubmed/37638448
http://dx.doi.org/10.3233/JND-230099

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657683/
https://www.ncbi.nlm.nih.gov/pubmed/37638448
http://dx.doi.org/10.3233/JND-230099

Ejemplares similares