Identification of a novel THAP1 mutation at R29 amino‐acid residue in sporadic patients with early‐onset dystonia
- 15 December 2009
- journal article
- letter
- Published by Wiley in Movement Disorders
- Vol. 24 (16) , 2428-2429
- https://doi.org/10.1002/mds.22849
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening studyThe Lancet Neurology, 2009
- Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening studyThe Lancet Neurology, 2009
- Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystoniaNature Genetics, 2009
- Dystonia in Parkinson’s diseaseZeitschrift für Neurologie, 2006