GeneticsbioRxivPreprint
Characterization of NEB mutations in patients reveals novel nemaline myopathy disease mechanisms and omecamtiv mecarbil force effects
Esmat Karimi, Mila van der Borgh, Johan Lindqvist…·Henk L. M. Granzier
This study characterizes NEB mutations in NEM2 patients, revealing mechanisms of nebulin dysfunction and the potential therapeutic benefit of Omecamtiv mecarbil.
3 citations