APA

Audo I., El Shamieh S., Méjécase C., Michiels C., Demontant V., Antonio A., Condroyer C., Boyard F., Letexier M., Saraiva J., Blanchard S., Mohand-Saïd S., Sahel J. & Zeitz C. (20180316). ARL2BP mutations account for 0.1% of autosomal recessive rod-cone dystrophies with the report of a novel splice variant. : Clinical genetics.

Chicago

Audo I, El Shamieh S, Méjécase C, Michiels C, Demontant V, Antonio A, Condroyer C, Boyard F, Letexier M, Saraiva J-P, Blanchard S, Mohand-Saïd S, Sahel J-A and Zeitz C. 20180316. ARL2BP mutations account for 0.1% of autosomal recessive rod-cone dystrophies with the report of a novel splice variant. : Clinical genetics.

Harvard

Audo I., El Shamieh S., Méjécase C., Michiels C., Demontant V., Antonio A., Condroyer C., Boyard F., Letexier M., Saraiva J., Blanchard S., Mohand-Saïd S., Sahel J. and Zeitz C. (20180316). ARL2BP mutations account for 0.1% of autosomal recessive rod-cone dystrophies with the report of a novel splice variant. : Clinical genetics.

MLA

Audo I, El Shamieh S, Méjécase C, Michiels C, Demontant V, Antonio A, Condroyer C, Boyard F, Letexier M, Saraiva J-P, Blanchard S, Mohand-Saïd S, Sahel J-A and Zeitz C. ARL2BP mutations account for 0.1% of autosomal recessive rod-cone dystrophies with the report of a novel splice variant. : Clinical genetics. 20180316.