Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5
Published inNeurology, vol. 70, no. 16 Pt 2, p. 1377-1383
Publication date2008
Abstract
Keywords
- Adult
- Aged
- Amino Acid Sequence
- Dystonia/drug therapy/genetics
- Female
- GTP Cyclohydrolase/genetics
- Humans
- Levodopa/therapeutic use
- Linkage (Genetics)/genetics
- Male
- Middle Aged
- Molecular Sequence Data
- Pedigree
- Quantitative Trait Loci/genetics
- Sequence Deletion/genetics
- Switzerland
Research group
Citation (ISO format)
WIDER, C. et al. Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5. In: Neurology, 2008, vol. 70, n° 16 Pt 2, p. 1377–1383. doi: 10.1212/01.wnl.0000275527.35752.c5
Main files (1)
Article (Accepted version)
Secondary files (2)
Identifiers
- PID : unige:1872
- DOI : 10.1212/01.wnl.0000275527.35752.c5
- PMID : 17804835
ISSN of the journal0028-3878