TY  - GEN
AU  - Kamm,C
AU  - Healy,D G
AU  - Quinn,N P
AU  - Wüllner,U
AU  - Moller,J C
AU  - Schols,L
AU  - Geser,F
AU  - Burk,K
AU  - Børglum,A D
AU  - Pellecchia,M T
AU  - Tolosa,E
AU  - del Sorbo,F
AU  - Nilsson,C
AU  - Bandmann,O
AU  - Sharma,M
AU  - Mayer,P
AU  - Gasteiger,M
AU  - Haworth,A
AU  - Ozawa,T
AU  - Lees,A J
AU  - Short,J
AU  - Giunti,P
AU  - Holinski-Feder,E
AU  - Illig,T
AU  - Wichmann,H E
AU  - Wenning,G K
AU  - Wood,N W
AU  - Gasser,T
TI  - The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group
SN  - 1460-2156
PY  - 2005///0816
KW  - Aged
KW  - Ataxia
KW  - complications
KW  - Cerebellar Ataxia
KW  - Cohort Studies
KW  - Diagnosis, Differential
KW  - Female
KW  - Fragile X Mental Retardation Protein
KW  - Fragile X Syndrome
KW  - Gene Frequency
KW  - Genotype
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Multiple System Atrophy
KW  - diagnosis
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - genetics
KW  - Peripheral Nervous System Diseases
KW  - RNA-Binding Proteins
KW  - Repetitive Sequences, Nucleic Acid
KW  - Tremor
N1  - Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/brain/awh535
ER  -