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HomeHealth NewsA protein-degradation mechanism opens a new treatment route for an inherited arrhythmia

A protein-degradation mechanism opens a new treatment route for an inherited arrhythmia

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The R33Q mutation in calsequestrin 2 (CASQ2) disrupts calcium control in heart cells and activates protein-degradation mechanisms. Credit: CNIC

An international team has identified a protein-degradation mechanism that contributes to the development of an inherited form of catecholaminergic polymorphic ventricular tachycardia (CPVT), a disease that mainly affects children and young people. The…

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