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Sense and Antisense DMPK RNA Foci Accumulate in DM1 Tissues during Development
Myotonic dystrophy type 1 (DM1) is caused by an unstable expanded CTG repeat located within the DMPK gene 3’UTR. The nature, severity and age at onset of DM1 symptoms are very variable in patients. Different forms of the disease are described, among which the congenital form (CDM) is the most severe...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Public Library of Science
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560382/ https://www.ncbi.nlm.nih.gov/pubmed/26339785 http://dx.doi.org/10.1371/journal.pone.0137620 |