NR AKKW
AU Satoh,A.; Goto,H.; Satoh,H.; Tomita,I.; Seto,M.; Furukawa,H.; Tsujihata,M.
TI A case of Creutzfeldt-Jakob disease with a point mutation at codon 232: correlation of MRI and neurologic findings.
QU Neurology 1997 Nov; 49(5): 1469-70
PT journal article
MH Case Report; Creutzfeldt-Jakob Syndrome/*diagnosis/*genetics; Female; Human; Magnetic Resonance Imaging; Middle Age; Neurologic Examination; *Point Mutation
AD Division of Neurology, Nagasaki Kita Hospital, Japan.
SP englisch
PO USA