NR AVPH
AU Rene,R.; Campdelacreu,J.; Ferrer,I.; Escrig,A.; Povedano,M.; Gascon-Bayarri,J.; Moral,E.
TI Familial Creutzfeldt-Jakob disease with E200K mutation presenting with neurosensorial hypoacusis
QU Journal of Neurology, Neurosurgery and Psychiatry 2007 Jan; 78(1): 103-4
PT case reports; letter; research support, non-u.s. gov't
MH Creutzfeldt-Jakob Syndrome/*complications/*genetics; Deafness/*etiology; Humans; Male; Middle Aged; Mutation; Pedigree; Polyneuropathies/*etiology; Prions/genetics
SP englisch
PO England