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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Bibliografski detalji
Izdano u:Genom Data
Glavni autori: Roberts, Thomas C., Blomberg, K. Emelie M., Smith, C.I. Edvard, EL Andaloussi, Samir, Wood, Matthew J.A.
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2015
Teme:
Data in Brief
Online pristup: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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