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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Detalhes bibliográficos
Publicado no:BMC Med Genomics
Main Authors: Markham, Larry W., Brinkmeyer-Langford, Candice L., Soslow, Jonathan H., Gupte, Manisha, Sawyer, Douglas B., Kornegay, Joe N., Galindo, Cristi L.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2017
Assuntos:
Research Article
Acesso em linha: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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