PRNP and variant Creutzfeldt-Jakob disease: Here, to investigate further the potential risks for transmission of cervid prions to humans, we have transmitted mule deer CWD prions to lines of transgenic mice overexpressing human PrP two- to sixfold with either methionine or valine at polymorphic residue 129 in which we have extensive experience of transmission of a wide range of human acquired, sporadic and inherited prion disease isolates, including kuru and multiple vCJD cases (Collinge et al., 1995a, b, 1996; Hill et al., 1997; Wadsworth et al., 2008a).