Open AccessCreutzfeldt-Jakob disease mortality in Canada, 1998 to 2013
Author(s) -
MB Coulthart,
GH Jansen,
Tim Connolly,
R D’Amour,
Jan Matthias Kruse,
Jennifer M. Lynch,
Stacy Sabourin,
Z Wang,
Antonio Giulivi,
M Ricketts,
NR Cashman
Publication year - 2015
Publication title -
canada communicable disease report
Language(s) - English
Resource type - Journals
eISSN - 1481-8531
pISSN - 1188-4169
DOI - 10.14745/ccdr.v41i08a01
Subject(s) - medicine , disease , confidence interval , public health , epidemiology , mortality rate , disease registry , creutzfeldt jakob syndrome , demography , pediatrics , disease surveillance , prion protein , pathology , sociology
Human prion diseases, known collectively as Creutzfeldt-Jakob disease (CJD), are fatal, infectious neurodegenerative disorders that occur in all human populations.
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