Myotonic Dystrophy
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical)
Reference110 articles.
1. Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland;Suominen;Eur J Hum Genet,2011
2. Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population;Norwood;Brain,2009
3. Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis;Siciliano;Clin Genet,2001
4. The epidemiology of myotonic dystrophy in Northern Ireland;Magee;Community Genet,1999
5. Myotonic dystrophy;Harper,2001
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1. Sleep Disorders and Fatigue in Patients with Different Forms of Myotonic Dystrophy Type 1;Neuroscience and Behavioral Physiology;2024-02-03
2. Normal-Pressure Hydrocephalus-Like Appearance in Myotonic Dystrophy Type 1;Cureus;2024-01-28
3. Combinatorial effects of ion channel mis-splicing as a cause of myopathy in myotonic dystrophy;Journal of Clinical Investigation;2024-01-02
4. Integrative Proteogenomics for Differential Expression and Splicing Variation in a DM1 Mouse Model;Molecular & Cellular Proteomics;2024-01
5. Pediatric Neuromuscular Diseases;Pediatric Neurology;2023-12
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