APA

Fradin M., Colin E., Hannouche-Bared D., Audo I., Sahel J. A., Biskup S., Carré W., Ziegler A., Wilhelm C., Guichet A., Odent S. & Bonneau D. (20171117). Run of homozygosity analysis reveals a novel nonsense variant of the CNGB1 gene involved in retinitis pigmentosa 45. : Ophthalmic genetics.

Chicago

Fradin Mélanie, Colin Estelle, Hannouche-Bared Daniele, Audo Isabelle, Sahel Jose Alain, Biskup Saskia, Carré Wilfried, Ziegler Alban, Wilhelm Christian, Guichet Agnès, Odent Sylvie and Bonneau Dominique. 20171117. Run of homozygosity analysis reveals a novel nonsense variant of the CNGB1 gene involved in retinitis pigmentosa 45. : Ophthalmic genetics.

Harvard

Fradin M., Colin E., Hannouche-Bared D., Audo I., Sahel J. A., Biskup S., Carré W., Ziegler A., Wilhelm C., Guichet A., Odent S. and Bonneau D. (20171117). Run of homozygosity analysis reveals a novel nonsense variant of the CNGB1 gene involved in retinitis pigmentosa 45. : Ophthalmic genetics.

MLA

Fradin Mélanie, Colin Estelle, Hannouche-Bared Daniele, Audo Isabelle, Sahel Jose Alain, Biskup Saskia, Carré Wilfried, Ziegler Alban, Wilhelm Christian, Guichet Agnès, Odent Sylvie and Bonneau Dominique. Run of homozygosity analysis reveals a novel nonsense variant of the CNGB1 gene involved in retinitis pigmentosa 45. : Ophthalmic genetics. 20171117.