APA

Gerber S., Hanein S., Perrault I., Delphin N., Aboussair N., Leowski C., Dufier J., Roche O., Munnich A., Kaplan J. & Rozet J. (20080128). Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II. : Human mutation.

Chicago

Gerber Sylvie, Hanein Sylvain, Perrault Isabelle, Delphin Nathalie, Aboussair Nisrine, Leowski Corinne, Dufier Jean-Louis, Roche Olivier, Munnich Arnold, Kaplan Josseline and Rozet Jean-Michel. 20080128. Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II. : Human mutation.

Harvard

Gerber S., Hanein S., Perrault I., Delphin N., Aboussair N., Leowski C., Dufier J., Roche O., Munnich A., Kaplan J. and Rozet J. (20080128). Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II. : Human mutation.

MLA

Gerber Sylvie, Hanein Sylvain, Perrault Isabelle, Delphin Nathalie, Aboussair Nisrine, Leowski Corinne, Dufier Jean-Louis, Roche Olivier, Munnich Arnold, Kaplan Josseline and Rozet Jean-Michel. Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II. : Human mutation. 20080128.