Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor
Open Access
- 31 May 2009
- journal article
- research article
- Published by Elsevier in Parkinsonism & Related Disorders
- Vol. 15 (4) , 321-323
- https://doi.org/10.1016/j.parkreldis.2008.06.010
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Reappraisal of the role of the DRD3 gene in essential tremorParkinsonism & Related Disorders, 2008
- Neuropathological changes in essential tremor: 33 cases compared with 21 controlsBrain, 2007
- Genetics of essential tremorBrain, 2007
- Study of possible factors associated with age of onset in essential tremorMovement Disorders, 2006
- Genetic analysis of the GABRA1 gene in patients with essential tremorNeuroscience Letters, 2006
- Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardationJournal of Medical Genetics, 2006
- Familial essential tremor with apparent autosomal dominant inheritance: Should we also consider other inheritance modes?Movement Disorders, 2006
- Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2Human Molecular Genetics, 2006
- Sodium channel mutations in epilepsy and other neurological disordersJournal of Clinical Investigation, 2005
- Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functionsGenetica, 2004