TY  - GEN
AU  - Ghanim,Mustapha
AU  - Guillot-Noel,Léna
AU  - Pasquier,Florence
AU  - Jornea,Ludmila
AU  - Deramecourt,Vincent
AU  - Dubois,Bruno
AU  - Le Ber,Isabelle
AU  - Brice,Alexis
TI  - CHMP2B mutations are rare in French families with frontotemporal lobar degeneration
SN  - 1432-1459
PY  - 2011///1110
KW  - Endosomal Sorting Complexes Required for Transport
KW  - genetics
KW  - Female
KW  - Frontotemporal Lobar Degeneration
KW  - diagnosis
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mutation, Missense
KW  - Pedigree
KW  - Phenotype
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1007/s00415-010-5655-8
ER  -