Pathogenic mechanism of a human mitochondrial [tRNA.sup.Phe] mutation associated with myoclonic epilepsy with ragged red fibers syndrome

MLA

Ling, Jiqiang, et al. “Pathogenic Mechanism of a Human Mitochondrial [TRNA.Sup.Phe] Mutation Associated with Myoclonic Epilepsy with Ragged Red Fibers Syndrome.” Proceedings of the National Academy of Sciences of the United States, vol. 104, no. 39, Sept. 2007, p. 15299. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsggo&AN=edsgcl.169677530&authtype=sso&custid=ns315887.

APA

Ling, J., Roy, H., Qin, D., Rubio, M. A. T., Alfonzo, J. D., Frederick, K., & Ibba, M. (2007). Pathogenic mechanism of a human mitochondrial [tRNA.sup.Phe] mutation associated with myoclonic epilepsy with ragged red fibers syndrome. Proceedings of the National Academy of Sciences of the United States, 104(39), 15299.

Chicago

Ling, Jiqiang, Herve Roy, Daoming Qin, Mary Anne T. Rubio, Juan D. Alfonzo, Kurt Frederick, and Michael Ibba. 2007. “Pathogenic Mechanism of a Human Mitochondrial [TRNA.Sup.Phe] Mutation Associated with Myoclonic Epilepsy with Ragged Red Fibers Syndrome.” Proceedings of the National Academy of Sciences of the United States 104 (39): 15299. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsggo&AN=edsgcl.169677530&authtype=sso&custid=ns315887.