APA

Ye D., Tester D. J., Zhou W., Papagiannis J. & Ackerman M. J. (20201002). A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel. : Heart rhythm.

Chicago

Ye Dan, Tester David J, Zhou Wei, Papagiannis John and Ackerman Michael J. 20201002. A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel. : Heart rhythm.

Harvard

Ye D., Tester D. J., Zhou W., Papagiannis J. and Ackerman M. J. (20201002). A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel. : Heart rhythm.

MLA

Ye Dan, Tester David J, Zhou Wei, Papagiannis John and Ackerman Michael J. A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel. : Heart rhythm. 20201002.