Molecular Genetics of Essential Tremor

Author:

Houle Gabrielle,Dion Patrick A,Rouleau Guy A

Publisher

Wiley

Reference54 articles.

1. Essential tremor: functional disability vs. subjective impairment;Auff E;Journal of Neural Transmission. Supplementum,1991

2. SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy;Bergareche A;Human Molecular Genetics,2015

3. Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease

4. Lrrk2 R1628P variant is a risk factor for essential tremor

5. Essential tremor linked TENM4 mutation found in healthy Chinese individuals

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