APA

Pingault V., Bodereau V., Baral V., Marcos S., Watanabe Y., Chaoui A., Fouveaut C., Leroy C., Vérier-Mine O., Francannet C., Dupin-Deguine D., Archambeaud F., Kurtz F., Young J., Bertherat J., Marlin S., Goossens M., Hardelin J., Dodé C. & Bondurand N. (20130705). Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness. : American journal of human genetics.

Chicago

Pingault Veronique, Bodereau Virginie, Baral Viviane, Marcos Severine, Watanabe Yuli, Chaoui Asma, Fouveaut Corinne, Leroy Chrystel, Vérier-Mine Odile, Francannet Christine, Dupin-Deguine Delphine, Archambeaud Françoise, Kurtz François-Joseph, Young Jacques, Bertherat Jérôme, Marlin Sandrine, Goossens Michel, Hardelin Jean-Pierre, Dodé Catherine and Bondurand Nadege. 20130705. Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness. : American journal of human genetics.

Harvard

Pingault V., Bodereau V., Baral V., Marcos S., Watanabe Y., Chaoui A., Fouveaut C., Leroy C., Vérier-Mine O., Francannet C., Dupin-Deguine D., Archambeaud F., Kurtz F., Young J., Bertherat J., Marlin S., Goossens M., Hardelin J., Dodé C. and Bondurand N. (20130705). Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness. : American journal of human genetics.

MLA

Pingault Veronique, Bodereau Virginie, Baral Viviane, Marcos Severine, Watanabe Yuli, Chaoui Asma, Fouveaut Corinne, Leroy Chrystel, Vérier-Mine Odile, Francannet Christine, Dupin-Deguine Delphine, Archambeaud Françoise, Kurtz François-Joseph, Young Jacques, Bertherat Jérôme, Marlin Sandrine, Goossens Michel, Hardelin Jean-Pierre, Dodé Catherine and Bondurand Nadege. Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness. : American journal of human genetics. 20130705.