GRMD cardiac and skeletal muscle metabolism gene profiles are distinct

BACKGROUND: Duchenne muscular dystrophy (DMD) is caused by mutations in the DMD gene, which codes for the dystrophin protein. While progress has been made in defining the molecular basis and pathogenesis of DMD, major gaps remain in understanding mechanisms that contribute to the marked delay in car...

Descripción completa

Detalles Bibliográficos
Autores principales: Markham, Larry W., Brinkmeyer-Langford, Candice L., Soslow, Jonathan H., Gupte, Manisha, Sawyer, Douglas B., Kornegay, Joe N., Galindo, Cristi L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385041/
https://www.ncbi.nlm.nih.gov/pubmed/28390424
http://dx.doi.org/10.1186/s12920-017-0257-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385041/
https://www.ncbi.nlm.nih.gov/pubmed/28390424
http://dx.doi.org/10.1186/s12920-017-0257-2

Ejemplares similares