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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Détails bibliographiques
Publié dans:Proc Natl Acad Sci U S A
Auteurs principaux: 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
Format: Artigo
Langue:Inglês
Publié: National Academy of Sciences 2018
Sujets:
Biological Sciences
Accès en ligne: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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