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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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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2013
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| Matèries: | |
| Accés en línia: | 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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