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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Bibliografiske detaljer
Udgivet i:Genom Data
Main Authors: Roberts, Thomas C., Blomberg, K. Emelie M., Smith, C.I. Edvard, EL Andaloussi, Samir, Wood, Matthew J.A.
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 2015
Fag:
Data in Brief
Online adgang: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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