Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt–Jakob disease patients
Keywords: CJD, Creutzfeldt–Jakob disease; PrP, prion protein; TSEs, transmissible spongiform encephalopathies; GSS, Gerstmann–Sträussler–Scheinker disease; PRNP, PrP gene; SDS–PAGE, sodium dodecyl sulphate polyacrylamide gel electrophoresis; DTT, dithiothreitol; CN