Article
Activation of the cGAS-STING pathway mediated by Irgm1 contributes to the development of restrictive cardiomyopathy induced by cTnIR193H mutation
2025-04-04
Abstract excerpt
<title>Abstract</title> <p>Restrictive cardiomyopathy (RCM) is a rare, fatal disorder that rapidly progresses in children. TNNI3 mutations represent the most common genetic cause. Although cTnI mutations are known to increase myofilament calcium sensitivity and impair diastolic function, this mechanism alone does not fully account for disease pathogenesis. Recent studies have revealed that the immune system plays...
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Identifiers and source
- Literature Corpus work
- 9961d2af-08a7-5490-9948-5e9c42ad4f67
- DOI
- 10.21203/rs.3.rs-6200397/v1
