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Autor:
Daisy Bougard, Maxime Bélondrade, Charly Mayran, Lilian Bruyère-Ostells, Sylvain Lehmann, Chantal Fournier-Wirth, Richard S. Knight, Robert G. Will, Alison J.E. Green
Publikováno v:
Emerging Infectious Diseases, Vol 24, Iss 7, Pp 1364-1366 (2018)
A patient with a heterozygous variant of Creutzfeldt-Jakob disease (CJD) with a methionine/valine genotype at codon 129 of the prion protein gene was recently reported. Using an ultrasensitive and specific protein misfolding cyclic amplification–ba
Externí odkaz:
https://doaj.org/article/8150508ff793474da938b30f687519fe