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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030307/
https://www.ncbi.nlm.nih.gov/pubmed/27708560
http://dx.doi.org/10.3389/fnins.2016.00428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030307/
https://www.ncbi.nlm.nih.gov/pubmed/27708560
http://dx.doi.org/10.3389/fnins.2016.00428

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