Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology

Although the genetic basis of Tourette Syndrome (TS) remains unclear, several candidate genes have been implicated. Using a set of 382 TS individuals of European ancestry we investigated four candidate genes for TS (HDC, SLITRK1, BTBD9, and SLC6A4) in an effort to identify possibly causal variants u...

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Pubblicato in:Front Neurosci
Autori principali: Alexander, John, Potamianou, Hera, Xing, Jinchuan, Deng, Li, Karagiannidis, Iordanis, Tsetsos, Fotis, Drineas, Petros, Tarnok, Zsanett, Rizzo, Renata, Wolanczyk, Tomasz, Farkas, Luca, Nagy, Peter, Szymanska, Urszula, Androutsos, Christos, Tsironi, Vaia, Koumoula, Anastasia, Barta, Csaba, Sandor, Paul, Barr, Cathy L., Tischfield, Jay, Paschou, Peristera, Heiman, Gary A., Georgitsi, Marianthi
Natura: Artigo
Lingua:Inglês
Pubblicazione: Frontiers Media S.A. 2016
Soggetti:
Neuroscience
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5030307/
https://ncbi.nlm.nih.gov/pubmed/27708560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2016.00428
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