Quantitative magnetic resonance imaging assessment of muscle composition in myotonic dystrophy mice

Myotonic dystrophy type 1 (DM1) is a severe autosomal dominant neuromuscular disease in which the musculoskeletal system contributes substantially to overall mortality and morbidity. DM1 stems from a noncoding CTG trinucleotide repeat expansion in the DMPK gene. The human skeletal actin long repeat...

Descripción completa

Detalles Bibliográficos
Autores principales: Bargiela, Ariadna, Ten-Esteve, Amadeo, Martí-Bonmatí, Luis, Sevilla, Teresa, Perez Alonso, Manuel, Artero, Ruben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831979/
https://www.ncbi.nlm.nih.gov/pubmed/36627397
http://dx.doi.org/10.1038/s41598-023-27661-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831979/
https://www.ncbi.nlm.nih.gov/pubmed/36627397
http://dx.doi.org/10.1038/s41598-023-27661-w

Ejemplares similares