TY  - GEN
AU  - Biancalana,Valérie
AU  - Toft,Mathias
AU  - Le Ber,Isabelle
AU  - Tison,François
AU  - Scherrer,Elisabeth
AU  - Thibodeau,Stephen
AU  - Mandel,Jean Louis
AU  - Brice,Alexis
AU  - Farrer,Matthew J
AU  - Dürr,Alexandra
TI  - FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy
SN  - 0003-9942
PY  - 2005///0630
KW  - Adult
KW  - Aged
KW  - Alleles
KW  - Cerebellar Ataxia
KW  - complications
KW  - Female
KW  - Fragile X Mental Retardation Protein
KW  - Fragile X Syndrome
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Multiple System Atrophy
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - genetics
KW  - Olivopontocerebellar Atrophies
KW  - RNA-Binding Proteins
KW  - Tremor
N1  - Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1001/archneur.62.6.962
ER  -