Mitochondrial tRNA mutations in Chinese children with tic disorders

Aim: To conduct the clinical, genetic, and molecular characterization of 494 Han Chinese subjects with tic disorders (TD). Methods: In the present study, we performed the mutational analysis of 22 mitochondrial tRNA genes in a large cohort of 494 Han Chinese subjects with TD via Sanger sequencing. T...

Descripción completa

Detalles Bibliográficos
Autores principales: Jiang, Peifang, Ling, Yinjie, Zhu, Tao, Luo, Xiaoying, Tao, Yilin, Meng, Feilong, Cheng, Weixin, Ji, Yanchun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Mutation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755120/
https://www.ncbi.nlm.nih.gov/pubmed/33289513
http://dx.doi.org/10.1042/BSR20201856

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755120/
https://www.ncbi.nlm.nih.gov/pubmed/33289513
http://dx.doi.org/10.1042/BSR20201856

Ejemplares similares