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Updated: Jan 14, 2026

Functional Characterization of Endogenously Expressed Human RYR1 Variants
Published on: June 9, 2021
Respiratory Failure Associated With Mutations in the RYR1 Gene: A Case Report
Chenliang Zhao1, Yongxiang Li2, Jinhui Li3
1Department of Critical Care Medicine Heyou Hospital Foshan City Guangdong P.R. China.
None:
A novel RYR1 mutation (c.C5701T:p.Q1901X) was identified in a 51-year-old female presenting with acute respiratory failure as the primary manifestation of congenital myopathy. This case expands the genotype-phenotype spectrum of RYR1-related myopathies and demonstrates that multidisciplinary intervention-including ventilator support, tracheostomy, and targeted rehabilitation-can significantly improve functional outcomes in late-onset cases.
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