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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...
Autores principales: | Markham, Larry W., Brinkmeyer-Langford, Candice L., Soslow, Jonathan H., Gupte, Manisha, Sawyer, Douglas B., Kornegay, Joe N., Galindo, Cristi L. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
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 |
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