APA

Perrault I., Delphin N., Hanein S., Gerber S., Dufier J., Roche O., Defoort-Dhellemmes S., Dollfus H., Fazzi E., Munnich A., Kaplan J. & Rozet J. (20070501). Spectrum of NPHP6/CEP290 mutations in Leber congenital amaurosis and delineation of the associated phenotype. : Human mutation.

Chicago

Perrault Isabelle, Delphin Nathalie, Hanein Sylvain, Gerber Sylvie, Dufier Jean-Louis, Roche Olivier, Defoort-Dhellemmes Sabine, Dollfus Hélène, Fazzi Elisa, Munnich Arnold, Kaplan Josseline and Rozet Jean-Michel. 20070501. Spectrum of NPHP6/CEP290 mutations in Leber congenital amaurosis and delineation of the associated phenotype. : Human mutation.

Harvard

Perrault I., Delphin N., Hanein S., Gerber S., Dufier J., Roche O., Defoort-Dhellemmes S., Dollfus H., Fazzi E., Munnich A., Kaplan J. and Rozet J. (20070501). Spectrum of NPHP6/CEP290 mutations in Leber congenital amaurosis and delineation of the associated phenotype. : Human mutation.

MLA

Perrault Isabelle, Delphin Nathalie, Hanein Sylvain, Gerber Sylvie, Dufier Jean-Louis, Roche Olivier, Defoort-Dhellemmes Sabine, Dollfus Hélène, Fazzi Elisa, Munnich Arnold, Kaplan Josseline and Rozet Jean-Michel. Spectrum of NPHP6/CEP290 mutations in Leber congenital amaurosis and delineation of the associated phenotype. : Human mutation. 20070501.