Abstract
Investigating the molecular disease mechanisms of the human p.G592R PRKD1 mutation in human induced pluripotent stem cell-derived cardiomyocytes
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
