Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders
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By jhenin
28 / Mar / 2017
Title | Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders |
Publication Type | Journal Article |
Year of Publication | 2012 |
Authors | Peoc'h K, Levavasseur E, Delmont E, Laffont-Proust ADe Simone, Privat N, Chebaro Y, Bedoucha CChapuis Pi, Brandel J-P, Laquerriere A, Hauw J-LKemeny Jea, Borg M, Rezaei H, Laplanche PDerreumaux, Haïk S |
Journal | Hum. Mol. Genet. |
Volume | 21 |
Pagination | 5417–5428 |
Date Published | dec |
DOI | 10.1093/hmg/dds377 |
Citation Key | 2012|1813 |