QuickView for MYL3;jsessionid=1470D6F611389BAE4F2936EFE54E6ACA (gene)

1. Mutation of the MYL3 gene in a patient with mid-ventricular obstructive hypertrophic cardiomyopathy.
2. Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3.
3. Ameliorating effect of rutin against diclofenac-induced cardiac injury in rats with underlying funct…
4. Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Car…
5. Molecular cloning and mRNA expression analysis of sheep MYL3 and MYL4 genes.

There were no clinical trials for MYL3;jsessionid=1470D6F611389BAE4F2936EFE54E6ACA