Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy | European Journal of Human Genetics
Kit-uri Smart myL2: solutii ideale pentru siguranta si confortul locuintei tale – myL2 Connect Blog – Automatizari case inteligente
Comparison of myofibril sarcomere structure between MYL2-R58Q iPSC-CMs... | Download Scientific Diagram
Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy | PLOS Genetics
Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology | Circulation: Genomic and Precision Medicine
myL2: Smart Home - Smart Building - Smart Office
High Affinity and Specificity MYL2 Polyclonal Antibody E-AB-70328 at Elabscience.com