Expanded CUG Repeat RNA Induces Premature Senescence in Myotonic Dystrophy Model Cells
Myotonic dystrophy type 1 (DM1) is a dominantly inherited disorder due to a toxic gain of function of RNA transcripts containing expanded CUG repeats (CUGexp). Patients with DM1 present with multisystemic symptoms, such as muscle wasting, cognitive impairment, cataract, frontal baldness, and endocri...
Prif Awduron: | , , |
---|---|
Fformat: | Erthygl |
Iaith: | English |
Cyhoeddwyd: |
Frontiers Media S.A.
2022-03-01
|
Cyfres: | Frontiers in Genetics |
Pynciau: | |
Mynediad Ar-lein: | https://www.frontiersin.org/articles/10.3389/fgene.2022.865811/full |