Open AccessSubstitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders
Author(s) -
K. Peoc'h,
E. Levavasseur,
E. Delmont,
A. De Simone,
I. Laffont-Proust,
N. Privat,
Y. Chebaro,
C. Chapuis,
P. Bedoucha,
J.-P. Brandel,
A. Laquerriere,
J.-L. Kemeny,
J.-J. Hauw,
M. Borg,
H. Rezaei,
P. Derreumaux,
J.-L. Laplanche,
S. Haik
Publication year - 2014
Publication title -
human molecular genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.811
H-Index - 276
eISSN - 1460-2083
pISSN - 0964-6906
DOI - 10.1093/hmg/ddt654
Subject(s) - biology , mechanism (biology) , prion protein , genetics , residue (chemistry) , neuroscience , disease , biochemistry , pathology , physics , medicine , quantum mechanics
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