APA

Venkateswaran S., Myers K. A., Smith A. C., Beaulieu C. L., Schwartzentruber J. A., Majewski J., Bulman D., Boycott K. M. & Dyment D. A. (20140922). Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation. : Epilepsia.

Chicago

Venkateswaran Sunita, Myers Ken A, Smith Amanda C, Beaulieu Chandree L, Schwartzentruber Jeremy A, Majewski Jacek, Bulman Dennis, Boycott Kym M and Dyment David A. 20140922. Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation. : Epilepsia.

Harvard

Venkateswaran S., Myers K. A., Smith A. C., Beaulieu C. L., Schwartzentruber J. A., Majewski J., Bulman D., Boycott K. M. and Dyment D. A. (20140922). Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation. : Epilepsia.

MLA

Venkateswaran Sunita, Myers Ken A, Smith Amanda C, Beaulieu Chandree L, Schwartzentruber Jeremy A, Majewski Jacek, Bulman Dennis, Boycott Kym M and Dyment David A. Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation. : Epilepsia. 20140922.