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Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I
In a recent issue of PLOS Genetics, we reported that the double-stranded RNA-binding protein, Staufen1, functions as a disease modifier in the neuromuscular disorder Myotonic Dystrophy Type I (DM1). In this work, we demonstrated that Staufen1 regulates the alternative splicing of exon 11 of the huma...
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| Publicado en: | Rare Dis |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Taylor & Francis
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5027583/ https://ncbi.nlm.nih.gov/pubmed/27695661 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/21675511.2016.1225644 |
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