A Rare Novel CLCN2 Variation and Risk of Gilles de la Tourette Syndrome: Whole-Exome Sequencing in a Multiplex Family and a Follow-Up Study in a Chinese Population

Rare inherited variations in multiplex families with Gilles de la Tourette syndrome (GTS) are suggested to play an important role in the genetic etiology of GTS. In order to explore the rare inherited variations with the risk of GTS, whole-exome sequencing (WES) was performed in a family with three...

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Detalles Bibliográficos
Autores principales: Yuan, Aihua, Wang, Zengge, Xu, Wen, Ding, Qiang, Zhao, Ying, Han, Jingjing, Sun, Jinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Psychiatry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744286/
https://www.ncbi.nlm.nih.gov/pubmed/33343406
http://dx.doi.org/10.3389/fpsyt.2020.543911

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744286/
https://www.ncbi.nlm.nih.gov/pubmed/33343406
http://dx.doi.org/10.3389/fpsyt.2020.543911

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