ASH1L may contribute to the risk of Tourette syndrome: Combination of family‐based analysis and case–control study

OBJECTIVE: Tourette syndrome (TS) is a childhood neurodevelopmental disorder caused by various genetic and environmental factors and presents with apparent genetic heterogeneity. As ASH1L potentially contributes to neurodevelopmental diseases, especially in TS, we aim to investigate the susceptibili...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Wenmiao, Xu, Lulu, Zhang, Cheng, Shen, Lu, Dong, Jicheng, Zhang, Han, Liu, Shiguo, Che, Fengyuan, Zheng, Xueping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014991/
https://www.ncbi.nlm.nih.gov/pubmed/35307981
http://dx.doi.org/10.1002/brb3.2539

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014991/
https://www.ncbi.nlm.nih.gov/pubmed/35307981
http://dx.doi.org/10.1002/brb3.2539

Ejemplares similares