Update on RYR1-related myopathies
Masashi Ogasawaraa and Ichizo Nishino
Purpose of Review
RYR1-related myopathy (RYR1-RM) is a group of myopathies caused by mutations in the RYR1 gene, which encodes the ryanodine receptor 1 (RYR1). This review discusses recent advances in the clinical features, pathology, pathogenesis, and therapeutics of RYR1-RM.
