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 (2012) - Comments
doi: 10.1093/hmg/dds377  issn: 1460-2083  issn: 0964-6906  pubmed: 22965875 

Katell Peoc'h, Etienne Levavasseur, Emilien Delmont, Alfonso De Simone, Isabelle Laffont-Proust, Nicolas Privat, Yassmine Chebaro, Céline Chapuis, Pierre Bedoucha, Jean-Philippe Brandel, Annie Laquerriere, Jean-Louis Kemeny, Jean-Jacques Hauw, Michel Borg, Human Rezaei, Philippe Derreumaux, Jean-Louis Laplanche, Stéphane Haïk