TY  - GEN
AU  - Bernardi,Livia
AU  - Cupidi,Chiara
AU  - Frangipane,Francesca
AU  - Anfossi,Maria
AU  - Gallo,Maura
AU  - Conidi,Maria Elena
AU  - Vasso,Franca
AU  - Colao,Rosanna
AU  - Puccio,Gianfranco
AU  - Curcio,Sabrina A M
AU  - Mirabelli,Maria
AU  - Clodomiro,Alessandra
AU  - Di Lorenzo,Raffaele
AU  - Smirne,Nicoletta
AU  - Maletta,Raffaele
AU  - Bruni,Amalia C
TI  - Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome
SN  - 1558-1497
PY  - 2015///1019
KW  - Aged
KW  - Female
KW  - Frontotemporal Lobar Degeneration
KW  - diagnosis
KW  - Genetic Association Studies
KW  - Genetic Testing
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mutation, Missense
KW  - Prions
KW  - genetics
KW  - Protein Structure, Tertiary
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/j.neurobiolaging.2014.06.006
ER  -