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Circulating Biomarkers for Duchenne Muscular Dystrophy
Duchenne muscular dystrophy is the most common form of muscular dystrophy. Genetic and biochemical research over the years has characterized the cause, pathophysiology and development of the disease providing several potential therapeutic targets and/or biomarkers. High throughput – omic technologie...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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IOS Press
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5271432/ https://www.ncbi.nlm.nih.gov/pubmed/27858763 http://dx.doi.org/10.3233/JND-150102 |