Expanding the phenotype of fragile X-associated tremor/ataxia syndrome: a new female case
Published in
Movement disorders, vol. 22, no. 11, p. 1677-1678Publication date
2007Keywords
- Aged
- Ataxia/etiology/genetics/pathology
- Female
- Fragile X Mental Retardation Protein/genetics
- Fragile X Syndrome/complications/genetics
- Humans
- Magnetic Resonance Imaging
- Mutation/genetics
- Phenotype
- Tremor/etiology/genetics/pathology
UNIGE research groups
Citation (ISO format)
HORVATH, Judit et al. Expanding the phenotype of fragile X-associated tremor/ataxia syndrome: a new female case. In: Movement disorders, 2007, vol. 22, n° 11, p. 1677–1678. doi: 10.1002/mds.21571
Main files (1)
Article (Published version)
Identifiers
- PID : unige:45494
- DOI : 10.1002/mds.21571
- PMID : 17516494
