Collins, S.J.

disease patient survival creutzfeldt –jakob disease creutzfeldt-jakob disease study codon protein prion brain creutzfeldt-jakob table creutzfeldt onset criteria diagnosis –jakob subtype analysis 14-3-3 control university surveillance department mutation speci ficity flair codon 129 signi erasmus university rotterdam 14-3-3 test neurol fication region signal gender nding month health sensitivity speci germany variant cjd scjd cases codon 129 genotype genotype neurology fi ndings atopic eczema number result ficity infant country imaging meissner mri scans sequence pattern prpsc effect variant collin signi ficantly signi ficance valine homozygote cases locus prion protein gene finite mri fi ndings prpsc type fluence homozygote valine caudate nucleus combination ratio eczema identi fication sanchez-juan