Harnessing molecular mechanism for precision medicine in dilated cardiomyopathy caused by a mutation in troponin T
L. Greenberg, W. T. Stump, Z. J. Lin, A. L. Bredemeyer, T. Blackwell, X. Hao, A. E. Greenberg, B. Garcia, K. Lavine, M. J. Greenberg
This study connects genotype, phenotype, and drug response in dilated cardiomyopathy using molecular mechanism-based computational and experimental approaches for a troponin T mutation.
bioRxiv · Apr 5, 2024 · PreprintBiophysics