Myotonic dystrophy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology
Reference55 articles.
1. A 10-year study of mortality in a cohort of patients with myotonic dystrophy
2. Myotonic dystrophy: Clinical and molecular parallels between myotonic dystrophy type 1 and type 2
3. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene
4. Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9
5. Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy
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1. A Selective Alkylating Agent for CTG Repeats in Myotonic Dystrophy Type 1;ACS Chemical Biology;2022-04-28
2. hnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologies;Muscle & Nerve;2021-03-22
3. The Biomarker Potential of miRNAs in Myotonic Dystrophy Type I;Journal of Clinical Medicine;2020-12-04
4. MyomiRNAs and myostatin as physical rehabilitation biomarkers for myotonic dystrophy;Neurological Sciences;2020-04-29
5. Pharmacological and physiological activation of AMPK improves the spliceopathy in DM1 mouse muscles;Human Molecular Genetics;2018-08-08
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