A de novo SCA14 mutation in an isolated case of late-onset cerebellar ataxia
- 12 July 2013
- journal article
- research article
- Published by Wiley in Movement Disorders
- Vol. 28 (13), 1902-1903
- https://doi.org/10.1002/mds.25572
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesNeurology, 2012
- PRKCG mutation (SCA‐14) causing a Ramsay Hunt phenotypeMovement Disorders, 2007
- The clinical and genetic spectrum of spinocerebellar ataxia 14Neurology, 2005
- Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia familyNeurology, 2003
- Genetic background of apparently idiopathic sporadic cerebellar ataxiaHuman Genetics, 2000