Premium
P3‐213: Progranulin Leu271LeufsX10 is one of the most common frontotemporal lobar degeneration and corticobasal syndrome associated mutations worldwide
Author(s) -
Benussi Luisa,
Ghidoni Roberta,
Pegoiani Eleonora,
Moretti Davide V.,
Zanetti Orazio,
Binetti Giuliano
Publication year - 2009
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2009.04.986
Subject(s) - frontotemporal lobar degeneration , frontotemporal dementia , progressive supranuclear palsy , c9orf72 , corticobasal degeneration , genetics , dementia , frameshift mutation , medicine , mutation , pathology , atrophy , biology , disease , gene
P3-213 PROGRANULIN LEU271LEUFSX10 IS ONE OF THE MOST COMMON FRONTOTEMPORAL LOBAR DEGENERATION AND CORTICOBASAL SYNDROME ASSOCIATED MUTATIONS WORLDWIDE Luisa Benussi, Roberta Ghidoni, Eleonora Pegoiani, Davide V. Moretti, Orazio Zanetti, Giuliano Binetti, NeuroBioGen Lab-Memory Clinic, IRCCS ‘‘S. Giovanni di Dio-FBF’’, Brescia, Italy; Proteomics Unit, IRCCS ‘‘Centro S. Giovanni di Dio-FBF’’, Brescia, Italy; Alzheimer Unit, IRCCS ‘‘S. Giovanni di Dio-FBF’’, Brescia, Italy. Contact e-mail: lbenussi@fatebenefratelli.it