K Schwartz

Base editing correction of hypertrophic cardiomyopathy in human cardiomyocytes and humanized mice

Mechanics and functional consequences of nuclear deformations

Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations

Autosomal dominant Emery–Dreifuss muscular dystrophy: a new family with late diagnosis