Stable Longitudinal Methylation Levels at the CpG Sites Flanking the CTG Repeat of <i>DMPK</i> in Patients with Myotonic Dystrophy Type 1
Myotonic dystrophy type 1 (DM1) is an autosomal dominant multisystem disorder mainly characterized by gradual muscle loss, weakness, and delayed relaxation after muscle contraction. It is caused by an expanded CTG repeat in the 3′ UTR of <i>DMPK</i>, which is transcribed into a toxic gai...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2020-08-01
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| Series: | Genes |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2073-4425/11/8/936 |