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Molecular mechanisms of muscle atrophy in myotonic dystrophies

Myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2) are multisystemic diseases that primarily affect skeletal muscle, causing myotonia, muscle atrophy, and muscle weakness. DM1 and DM2 pathologies are caused by expansion of CTG and CCTG repeats in non-coding regions of the genes enco...

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Kaydedildi:
Detaylı Bibliyografya
Yazar: Timchenko, Lubov
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3759660/
https://ncbi.nlm.nih.gov/pubmed/23796888
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biocel.2013.06.010
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