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An Overview of Alternative Splicing Defects Implicated in Myotonic Dystrophy Type I
Myotonic dystrophy type I (DM1) is the most common form of adult muscular dystrophy, caused by expansion of a CTG triplet repeat in the 3′ untranslated region (3′UTR) of the myotonic dystrophy protein kinase (DMPK) gene. The pathological CTG repeats result in protein trapping by expanded transcripts...
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| Publicado en: | Genes (Basel) |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
MDPI
2020
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7564762/ https://ncbi.nlm.nih.gov/pubmed/32971903 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11091109 |
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