TY  - JOUR
AU  - Diez-Fairen, Monica
AU  - Houle, Gabrielle
AU  - Ortega-Cubero, Sara
AU  - Bandres-Ciga, Sara
AU  - Alvarez, Ignacio
AU  - Carcel, Maria
AU  - Ibañez, Laura
AU  - Fernandez, Maria Victoria
AU  - Budde, John P
AU  - Trotta, Jean-Remi
AU  - Tonda, Raul
AU  - Chong, Jessica X
AU  - Bamshad, Michael J
AU  - Nickerson, Deborah A
AU  - Aguilar, Miquel
AU  - Tartari, Juan P
AU  - Gironell, Alexandre
AU  - Garcia-Martin, Elena
AU  - Agundez, Jose Ag
AU  - Alonso-Navarro, Hortensia
AU  - Jimenez-Jimenez, Felix Javier
AU  - Fernandez, Manel
AU  - Valldeoriola, Francesc
AU  - Marti, Maria Jose
AU  - Tolosa, Eduard
AU  - Coria, Francisco
AU  - Pastor, Maria A
AU  - Vilariño-Güell, Carles
AU  - Rajput, Alex
AU  - Dion, Patrick A
AU  - Cruchaga, Carlos
AU  - Rouleau, Guy A
AU  - Pastor, Pau
PY  - 2020
DO  - 10.1016/j.parkreldis.2020.11.021
UR  - http://hdl.handle.net/10668/16738
T2  - Parkinsonism & related disorders
AB  - Essential tremor (ET) is one of the most common movement disorders. Despite its high prevalence and heritability, its genetic etiology remains elusive with only a few susceptibility genes identified and poorly replicated. Our aim was to find novel...
LA  - en
PB  - Elsevier Ltd
KW  - Essential tremor
KW  - Genetic risk
KW  - MMP10
KW  - Rare variants
KW  - WES
KW  - Adult
KW  - Age of Onset
KW  - Aged
KW  - Aged, 80 and over
KW  - Essential Tremor
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - Male
KW  - Matrix Metalloproteinase 10
KW  - Middle Aged
KW  - Pedigree
KW  - Exome Sequencing
KW  - Young Adult
TI  - Exome-wide rare variant analysis in familial essential tremor.
TY  - research article
VL  - 82
ER  -