NR AFJV
AU Hillier,C.E.M.; Llewelyn,J.G.; Neal,J.W.; Ironside,J.W.
TI Creutzfeldt-Jakob disease in a young person with valine homozygosity at codon 129: sporadic or variant?
QU Journal of Neurology, Neurosurgery and Psychiatry 2001 Jan; 70(1): 134-5
PT letter
MH Adult; Case Report; Codon/genetics; Creutzfeldt-Jakob Syndrome/*genetics/*physiopathology; Homozygote; Human; Male; Valine/*genetics
SP englisch
PO England