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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...
Autores principales: | Hrach, Heather C., Mangone, Marco |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
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 |
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