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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Front Neurosci
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Frontiers Media S.A. 2016
Pynciau:
Neuroscience
Mynediad Ar-lein: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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