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...

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Detalhes bibliográficos
Publicado no:Biosci Rep
Main Authors: Jiang, Peifang, Ling, Yinjie, Zhu, Tao, Luo, Xiaoying, Tao, Yilin, Meng, Feilong, Cheng, Weixin, Ji, Yanchun
Formato: Artigo
Idioma:Inglês
Publicado em: Portland Press Ltd. 2020
Assuntos:
Mutation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7755120/
https://ncbi.nlm.nih.gov/pubmed/33289513
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BSR20201856
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