QuickView for MYL3;jsessionid=51D8FEDF7EC8F0849EB1CA10DF7EBC86 (gene)

1. Mutation of the MYL3 gene in a patient with mid-ventricular obstructive hypertrophic cardiomyopathy.
2. MYL3 protects chondrocytes from senescence by inhibiting clathrin-mediated endocytosis and activatin…
3. Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3.
4. Ameliorating effect of rutin against diclofenac-induced cardiac injury in rats with underlying funct…
5. Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Car…

There were no clinical trials for MYL3;jsessionid=51D8FEDF7EC8F0849EB1CA10DF7EBC86