Identification of Potential Biomarkers for Ryanodine Receptor 1 (RYR1) Mutation-Associated Myopathies Using Bioinformatics Approach

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 contributes to the management and preparation f...

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Detalles Bibliográficos
Autores principales: Wang, Xi, Kong, Chang, Liu, Pan, Geng, Wujun, Tang, Hongli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187445/
https://www.ncbi.nlm.nih.gov/pubmed/35692882
http://dx.doi.org/10.1155/2022/8787782

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187445/
https://www.ncbi.nlm.nih.gov/pubmed/35692882
http://dx.doi.org/10.1155/2022/8787782

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