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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Detalles Bibliográficos
Autores principales: Hrach, Heather C., Mangone, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769970/
https://www.ncbi.nlm.nih.gov/pubmed/31546754
http://dx.doi.org/10.3390/ijms20184638

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769970/
https://www.ncbi.nlm.nih.gov/pubmed/31546754
http://dx.doi.org/10.3390/ijms20184638

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