Clinical and genetic characteristics of childhood‐onset myotonic dystrophy
Author:
Affiliation:
1. Department of Pediatrics & Neurology, Division of Pediatric NeurologyThe University of Texas Southwestern Medical Center Dallas Texas
2. Children's Medical Center Dallas Dallas Texas
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.26716
Reference27 articles.
1. Congenital myotonic dystrophy in a national registry
2. Epidemiology of myotonic dystrophy type 1 (Steinert disease) in Belgrade (Serbia)
3. Autism spectrum conditons in myotonic dystrophy type 1: A study on 57 individuals with congenital and childhood forms
4. Cognitive impairment in myotonic dystrophy type 1 (DM1)
5. Long-term follow-up of patients with myotonic dystrophy: an electrocardiogram every year is not necessary
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1. The Study of the Inheritance Mechanisms of Myotonic Dystrophy Type 1 (DM1) in Families from the Republic of North Ossetia-Alania;International Journal of Molecular Sciences;2024-09-09
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3. CNS involvement in myotonic dystrophy type 1: does sex play a role?;Frontiers in Neurology;2024-05-09
4. Myotone Dystrophien, nichtdystrophe Myotonien und periodische Paralysen;DGNeurologie;2024-04-18
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