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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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Literature Corpus work
9961d2af-08a7-5490-9948-5e9c42ad4f67
DOI
10.21203/rs.3.rs-6200397/v1
Open publication

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Activation of the cGAS-STING pathway mediated by Irgm1 contributes to the development of restrictive cardiomyopathy induced by cTnIR193H mutationDOI 10.21203/rs.3.rs-6200397/v1
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