Exome-wide rare variant analysis in familial essential tremor

INTRODUCTION: Essential tremor (ET) is one of the most common movement disorders. Despite its high prevalence and heritability, its genetic aetiology remains elusive with only a few susceptibility genes identified and poorly replicated. Our aim was to find novel candidate genes involved in ET predis...

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Publicado no:Parkinsonism Relat Disord
Main Authors: Diez-Fairen, Monica, Houle, Gabrielle, Ortega-Cubero, Sara, Bandres-Ciga, Sara, Alvarez, Ignacio, Carcel, Maria, Ibañez, Laura, Fernandez, Maria Victoria, Budde, John P., Trotta, Jean-Rémi, Tonda, Raúl, Chong, Jessica X., Bamshad, Michael J., Nickerson, Deborah A., Aguilar, Miquel, Tartari, Juan P., Gironell, Alexandre, García-Martín, Elena, Agundez, Jose AG, Alonso-Navarro, Hortensia, Jimenez-Jimenez, Felix Javier, Fernandez, Manel, Valldeoriola, Francesc, Marti, Maria Jose, Tolosa, Eduard, Coria, Francisco, Pastor, Maria A., Vilariño-Güell, Carles, Rajput, Alex, Dion, Patrick A., Cruchaga, Carlos, Rouleau, Guy A., Pastor, Pau
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7856267/
https://ncbi.nlm.nih.gov/pubmed/33279834
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2020.11.021
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