Coding mutations in NUS1 contribute to Parkinson’s disease

Whole-exome sequencing has been successful in identifying genetic factors contributing to familial or sporadic Parkinson’s disease (PD). However, this approach has not been applied to explore the impact of de novo mutations on PD pathogenesis. Here, we sequenced the exomes of 39 early onset patients...

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Detalhes bibliográficos
Publicado no:Proc Natl Acad Sci U S A
Main Authors: Guo, Ji-feng, Zhang, Lu, Li, Kai, Mei, Jun-pu, Xue, Jin, Chen, Jia, Tang, Xia, Shen, Lu, Jiang, Hong, Chen, Chao, Guo, Hui, Wu, Xue-li, Sun, Si-long, Xu, Qian, Sun, Qi-ying, Chan, Piu, Shang, Hui-fang, Wang, Tao, Zhao, Guo-hua, Liu, Jing-yu, Xie, Xue-feng, Jiang, Yi-qi, Liu, Zhen-hua, Zhao, Yu-wen, Zhu, Zuo-bin, Li, Jia-da, Hu, Zheng-mao, Yan, Xin-xiang, Fang, Xiao-dong, Wang, Guang-hui, Zhang, Feng-yu, Xia, Kun, Liu, Chun-yu, Zhu, Xiong-wei, Yue, Zhen-yu, Li, Shuai Cheng, Cai, Huai-bin, Zhang, Zhuo-hua, Duan, Ran-hui, Tang, Bei-sha
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2018
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6233099/
https://ncbi.nlm.nih.gov/pubmed/30348779
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1809969115
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