Congenital myopathies and congenital muscular dystrophies
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Neurology
Reference70 articles.
1. A NEW CONGENITAL NON-PROGRESSIVE MYOPATHY
2. Central core disease and congenital neuromuscular disease with uniform type 1 fibers in one family
3. Central Core Disease
4. Ryanodine receptor mutations in malignant hyperthermia and central core disease
5. A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease
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