APA

Peoc'h K., Levavasseur E., Delmont E., De Simone A., Laffont-Proust I., Privat N., Chebaro Y., Chapuis C., Bedoucha P., Brandel J., Laquerriere A., Kemeny J., Hauw J., Borg M., Rezaei H., Derreumaux P., Laplanche J. & Haïk S. (20130515). Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders. : Human molecular genetics.

Chicago

Peoc'h Katell, Levavasseur Etienne, Delmont Emilien, De Simone Alfonso, Laffont-Proust Isabelle, Privat Nicolas, Chebaro Yassmine, Chapuis Céline, Bedoucha Pierre, Brandel Jean-Philippe, Laquerriere Annie, Kemeny Jean-Louis, Hauw Jean-Jacques, Borg Michel, Rezaei Human, Derreumaux Philippe, Laplanche Jean-Louis and Haïk Stéphane. 20130515. Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders. : Human molecular genetics.

Harvard

Peoc'h K., Levavasseur E., Delmont E., De Simone A., Laffont-Proust I., Privat N., Chebaro Y., Chapuis C., Bedoucha P., Brandel J., Laquerriere A., Kemeny J., Hauw J., Borg M., Rezaei H., Derreumaux P., Laplanche J. and Haïk S. (20130515). Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders. : Human molecular genetics.

MLA

Peoc'h Katell, Levavasseur Etienne, Delmont Emilien, De Simone Alfonso, Laffont-Proust Isabelle, Privat Nicolas, Chebaro Yassmine, Chapuis Céline, Bedoucha Pierre, Brandel Jean-Philippe, Laquerriere Annie, Kemeny Jean-Louis, Hauw Jean-Jacques, Borg Michel, Rezaei Human, Derreumaux Philippe, Laplanche Jean-Louis and Haïk Stéphane. Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders. : Human molecular genetics. 20130515.