Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor

OBJECTIVE: Sporadic, genetically complex essential tremor (ET) is one of the most common movement disorders and may lead to severe impairment of the quality of life. Despite high heritability, the genetic determinants of ET are largely unknown. We performed the second genome-wide association study (...

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Bibliografiset tiedot
Päätekijät: Thier, Sandra, Lorenz, Delia, Nothnagel, Michael, Poremba, Caroline, Papengut, Frank, Appenzeller, Silke, Paschen, Steffen, Hofschulte, Frank, Hussl, Anna-Christina, Hering, Sascha, Poewe, Werner, Asmus, Friedrich, Gasser, Thomas, Schöls, Ludger, Christensen, Kaare, Nebel, Almut, Schreiber, Stefan, Klebe, Stephan, Deuschl, Günther, Kuhlenbäumer, Gregor
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Lippincott Williams & Wilkins 2012
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Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3398434/
https://ncbi.nlm.nih.gov/pubmed/22764253
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e31825fdeed
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