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...

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Veröffentlicht in:BMC Med Genomics
Hauptverfasser: Markham, Larry W., Brinkmeyer-Langford, Candice L., Soslow, Jonathan H., Gupte, Manisha, Sawyer, Douglas B., Kornegay, Joe N., Galindo, Cristi L.
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2017
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5385041/
https://ncbi.nlm.nih.gov/pubmed/28390424
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-017-0257-2
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