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

Abstract 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 lon...

Full description

Bibliographic Details
Main Authors: Ariadna Bargiela, Amadeo Ten-Esteve, Luis Martí-Bonmatí, Teresa Sevilla, Manuel Perez Alonso, Ruben Artero
Format: Article
Language:English
Published: Nature Portfolio 2023-01-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-27661-w