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Next generation sequencing in neuromuscular diseases
PURPOSE OF REVIEW: Neuromuscular diseases are clinically and genetically heterogeneous and probably contains the greatest proportion of causative Mendelian defects than any other group of conditions. These disorders affect muscle and/or nerves with neonatal, childhood or adulthood onset, with signif...
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| Publicat a: | Curr Opin Neurol |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5082606/ https://ncbi.nlm.nih.gov/pubmed/27588584 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WCO.0000000000000374 |
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