The Limb-Girdle Muscular Dystrophies and the Dystrophinopathies
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics(clinical),Clinical Neurology
Reference25 articles.
1. A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield
2. Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy
3. myotilin Mutation Found in Second Pedigree with LGMD1A
4. Cardiac Involvement in Patients With Muscular Dystrophies
5. Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy
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