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Muscle wasting in myotonic dystrophies: a model of premature aging
Myotonic dystrophy type 1 (DM1 or Steinert’s disease) and type 2 (DM2) are multisystem disorders of genetic origin. Progressive muscular weakness, atrophy and myotonia are the most prominent neuromuscular features of these diseases, while other clinical manifestations such as cardiomyopathy, insulin...
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| Yayımlandı: | Front Aging Neurosci |
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| Asıl Yazarlar: | , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Frontiers Media S.A.
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4496580/ https://ncbi.nlm.nih.gov/pubmed/26217220 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnagi.2015.00125 |
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