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Congenital and childhood myotonic dystrophy: Current aspects of disease and future directions
Myotonic dystrophy type 1 (DM1) is multisystem disease arising from mutant CTG expansion in the non-translating region of the dystrophia myotonica protein kinase gene. While DM1 is the most common adult muscular dystrophy, with a worldwide prevalence of one in eight thousand, age of onset varies fro...
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| Publicado no: | World J Clin Pediatr |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Inc
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4637811/ https://ncbi.nlm.nih.gov/pubmed/26566479 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5409/wjcp.v4.i4.66 |
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