Mechanistic Basis for Type 2 Long QT Syndrome Caused by KCNH2 Mutations that Disrupt Conserved Arginine Residues in the Voltage Sensor
Titel:
Mechanistic Basis for Type 2 Long QT Syndrome Caused by KCNH2 Mutations that Disrupt Conserved Arginine Residues in the Voltage Sensor
Auteur:
McBride, Christie M. Smith, Ashley M. Smith, Jennifer L. Reloj, Allison R. Velasco, Ellyn J. Powell, Jonathan Elayi, Claude S. Bartos, Daniel C. Burgess, Don E. Delisle, Brian P.