The X‐linked Becker muscular dystrophy (bmx) mouse models Becker muscular dystrophy via deletion of murine dystrophin exons 45–47

BACKGROUND: Becker muscular dystrophy (BMD) is a genetic neuromuscular disease of growing importance caused by in‐frame, partial loss‐of‐function mutations in the dystrophin (DMD) gene. BMD presents with reduced severity compared with Duchenne muscular dystrophy (DMD), the allelic disorder of comple...

Descripción completa

Detalles Bibliográficos
Autores principales: Heier, Christopher R., McCormack, Nikki M., Tully, Christopher B., Novak, James S., Newell‐Stamper, Breanne L., Russell, Alan J., Fiorillo, Alyson A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067474/
https://www.ncbi.nlm.nih.gov/pubmed/36628607
http://dx.doi.org/10.1002/jcsm.13171

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067474/
https://www.ncbi.nlm.nih.gov/pubmed/36628607
http://dx.doi.org/10.1002/jcsm.13171

Ejemplares similares