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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Dettagli Bibliografici
Pubblicato in:Proc Natl Acad Sci U S A
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: National Academy of Sciences 2018
Soggetti:
Biological Sciences
Accesso online: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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