Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families.
Original article English Goldfarb LG, Brown P, Mitrova E, Cervenakova L, Goldin L, Korczyn AD, Chapman J, Galvez S, Cartier L, Rubenstein R, et al. Laboratory of CNS Studies, NINDS, NIH, Bethesda, MD 20892. Eur J Epidemiol. 1991 Sep;7(5):477-86. Abstract 200Lys mutation in the human PRNP coding region has been identified in 45 of the …