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Altered expression and splicing of Ca(2+) metabolism genes in myotonic dystrophies DM1 and DM2
AIMS: Myotonic dystrophy types 1 and 2 (DM1 and DM2) are multisystem disorders caused by similar repeat expansion mutations, with similar yet distinct clinical features. Aberrant splicing of multiple effector genes, as well as dysregulation of transcription and translation, have been suggested to un...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3882430/ https://ncbi.nlm.nih.gov/pubmed/22758909 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2990.2012.01289.x |
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