Myotonic dystrophies
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Neurology
Reference62 articles.
1. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
2. An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy
3. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene
4. Myotonic dystrophy with no trinucleotide repeat expansion
5. Proximal myotonic myopathy
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1. Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review;BMC Neurology;2020-02-12
2. Differences in the pattern of cognitive impairments between juvenile and adult onset myotonic dystrophy type 1;Journal of Clinical Neuroscience;2019-10
3. Gene therapy in monogenic congenital myopathies;Methods;2016-04
4. Gene Therapy in Monogenic Congenital Myopathies;Translating Regenerative Medicine to the Clinic;2016
5. Psychological characteristics of patients with myotonic dystrophy type 1;Acta Neurologica Scandinavica;2014-12-11
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