Whole exome sequencing identifies genes associated with Tourette’s Disorder in multiplex families

Tourette’s Disorder (TD) is a neurodevelopmental disorder that affects about 0.7% of the population and is one of the most heritable neurodevelopmental disorders. Nevertheless, because of its polygenic nature and genetic heterogeneity, the genetic etiology of TD is not well understood. In this study...

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Detalles Bibliográficos
Autores principales: Cao, Xiaolong, Zhang, Yeting, Abdulkadir, Mohamed, Deng, Li, Fernandez, Thomas V., Garcia-Delgar, Blanca, Hagstrøm, Julie, Hoekstra, Pieter J., King, Robert A., Koesterich, Justin, Kuperman, Samuel, Morer, Astrid, Nasello, Cara, Plessen, Kerstin J., Thackray, Joshua K., Zhou, Lisheng, Dietrich, Andrea, Tischfield, Jay A., Heiman, Gary A., Xing, Jinchuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501157/
https://www.ncbi.nlm.nih.gov/pubmed/33837273
http://dx.doi.org/10.1038/s41380-021-01094-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501157/
https://www.ncbi.nlm.nih.gov/pubmed/33837273
http://dx.doi.org/10.1038/s41380-021-01094-1

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