Fig. 1From: Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein genePRNP mutations. Single point mutations, stop-codon mutations, insertion and deletion mutations in the coding region of PRNP gene, which have been proposed as pathogenic variants of the prion protein. Polymorphisms or other genetic variations whose pathogenic value is unknown or uncertain are not reported in this figureBack to article page