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miRNA Profiling for Early Detection and Treatment of Duchenne Muscular Dystrophy

Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder caused by out of frame mutations in the dystrophin gene. The hallmark symptoms of the condition include progressive degeneration of skeletal muscle, cardiomyopathy, and respiratory dysfunction. The most recent advances in th...

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Detalhes bibliográficos
Publicado no:Int J Mol Sci
Main Authors: Hrach, Heather C., Mangone, Marco
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6769970/
https://ncbi.nlm.nih.gov/pubmed/31546754
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20184638
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