TY  - GEN
AU  - Rossi,Giacomina
AU  - Marelli,Cecilia
AU  - Farina,Laura
AU  - Laurà,Matilde
AU  - Maria Basile,Anna
AU  - Ciano,Claudia
AU  - Tagliavini,Fabrizio
AU  - Pareyson,Davide
TI  - The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome
SN  - 1531-8257
PY  - 2008///0806
KW  - Adult
KW  - Amino Acid Substitution
KW  - Basal Ganglia
KW  - pathology
KW  - Brain Diseases
KW  - genetics
KW  - Cerebral Cortex
KW  - Chromosomes, Human, Pair 17
KW  - Dementia
KW  - Humans
KW  - Male
KW  - Parkinson Disease
KW  - Tauopathies
KW  - Tremor
KW  - etiology
KW  - tau Proteins
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/mds.21970
ER  -