Campbell, T.A.

prion disease deletion octapeptide prion disease patient prion protein gene mutation protein region creutzfeldt-jakob disease insertion product prion diseases prion protein 348 base pairs dementia n-terminal isoform two-octapeptide allele 72 ° c diagnosis analysis onset neurol figure domain creutzfeldt-jakob minute collinge primers virus department sense wild-type allele neurology n-terminal domain integral numbers lanes 2 right side antibody cerebrospinal fluid replication slippage individual size fractionation reading frame kleinschmidt-demasters bk college school gilden pcr product mahal sp report antisense 94 ° c polymerase 53 ° c syndrome herpes zoster pseudodendrites novel disease mechanism mrc prion unit head ct scan varicellazoster virus meningoradiculitis guillain –barr syndrome octapeptide insertion mutations 3 rd ed frcp prion diseases varicella-zoster prion disease kindreds copper neurogenetic varicella-zoster virus antibody place n-terminal copper binding tremor varicella-zoster virus encephalitis c-terminal globular domain –insulin diabetes mellitus cause reading