mRNA and microRNA transcriptomics analyses in a murine model of dystrophin loss and therapeutic restoration

Duchenne muscular dystrophy (DMD) is a pediatric, X-linked, progressive muscle-wasting disorder caused by loss of function mutations affecting the gene encoding the dystrophin protein. While the primary genetic insult in DMD is well described, many details of the molecular and cellular pathologies t...

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Detalles Bibliográficos
Publicado en:Genom Data
Main Authors: Roberts, Thomas C., Blomberg, K. Emelie M., Smith, C.I. Edvard, EL Andaloussi, Samir, Wood, Matthew J.A.
Formato: Artigo
Idioma:Inglês
Publicado: Elsevier 2015
Assuntos:
Data in Brief
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4778658/
https://ncbi.nlm.nih.gov/pubmed/26981371
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gdata.2015.11.025
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