APA

Downs L. M., Scott E. M., Cideciyan A. V., Iwabe S., Dufour V., Gardiner K. L., Genini S., Marinho L. F., Sumaroka A., Kosyk M. S., Swider M., Aguirre G. K., Jacobson S. G., Beltran W. A. & Aguirre G. D. (20170609). Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutation. : Human molecular genetics.

Chicago

Downs Louise M, Scott Erin M, Cideciyan Artur V, Iwabe Simone, Dufour Valerie, Gardiner Kristin L, Genini Sem, Marinho Luis Felipe, Sumaroka Alexander, Kosyk Mychajlo S, Swider Malgorzata, Aguirre Geoffrey K, Jacobson Samuel G, Beltran William A and Aguirre Gustavo D. 20170609. Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutation. : Human molecular genetics.

Harvard

Downs L. M., Scott E. M., Cideciyan A. V., Iwabe S., Dufour V., Gardiner K. L., Genini S., Marinho L. F., Sumaroka A., Kosyk M. S., Swider M., Aguirre G. K., Jacobson S. G., Beltran W. A. and Aguirre G. D. (20170609). Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutation. : Human molecular genetics.

MLA

Downs Louise M, Scott Erin M, Cideciyan Artur V, Iwabe Simone, Dufour Valerie, Gardiner Kristin L, Genini Sem, Marinho Luis Felipe, Sumaroka Alexander, Kosyk Mychajlo S, Swider Malgorzata, Aguirre Geoffrey K, Jacobson Samuel G, Beltran William A and Aguirre Gustavo D. Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutation. : Human molecular genetics. 20170609.