Identification of Potential Biomarkers for Ryanodine Receptor 1 (RYR1) Mutation-Associated Myopathies Using Bioinformatics Approach
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DOI: 10.1155/2022/8787782
Abstract: Background Myopathies related to Ryanodine receptor 1 (RYR1) mutation are the most common nondystrophy muscle disorder in humans. Early detection and diagnosis of RYR1 mutation-associated myopathies may lead to more timely treatment of patients, which… read more here.
Keywords: associated myopathies; mutation associated; ryr1 mutation; mutation ... See more keywords