APA citiranje

den Hollander, A. I., Koenekoop, R. K., Yzer, S., Lopez, I., Arends, M. L., Voesenek, K. E. J., . . . Cremers, F. P. M. (2006). Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis. The American Society of Human Genetics.

Citação norma Chicago

den Hollander, Anneke I., et al. Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis. The American Society of Human Genetics, 2006.

MLA citiranje

den Hollander, Anneke I., et al. Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis. The American Society of Human Genetics, 2006.