(Q54093251)
Statements
A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. (English)
Gambetti P
Hainfellner JA
Kitamoto T
Jarius C
1 June 1999
45
6
812-816