Epigenetics of Myotonic Dystrophies: A Minireview
Myotonic dystrophy type 1 and 2 (DM1 and DM2) are two multisystemic autosomal dominant disorders with clinical and genetic similarities. The prevailing paradigm for DMs is that they are mediated by an <i>in trans</i> toxic RNA mechanism, triggered by untranslated CTG and CCTG repeat expa...
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| Autores principales: | , , , , , |
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| Formato: | article |
| Lenguaje: | EN |
| Publicado: |
MDPI AG
2021
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| Materias: | |
| Acceso en línea: | https://doaj.org/article/7ff44c4a9e6f4d79894d04671a5e1458 |
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