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	1.	Advances in detecting and reducing off-target effects generated by CRISPR-mediated genome editing. [electronic resource] by Li, Jinjing Hong, Shunyan Chen, Wanjin Zuo, Erwei Yang, Hui Producer: 20200720 In: Journal of genetics and genomics = Yi chuan xue bao vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson's disease in a Han-Chinese population in south-eastern China. [electronic resource] by Cai, Jiangping Lin, Yi Chen, Wanjin Lin, Qifang Cai, Bin Wang, Ning Zheng, Weihong Producer: 20140626 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Clinical and genetic investigation in Chinese patients with demyelinating Charcot-Marie-Tooth disease. [electronic resource] by He, Jin Guo, Lingling Xu, Guorong Xu, Liuqing Lin, Shan Chen, Wanjin Wang, Ning Producer: 20191021 In: Journal of the peripheral nervous system : JPNS vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Screening for FMR1 expanded alleles in patients with parkinsonism in mainland China. [electronic resource] by Zhang, Xiong Zhuang, Xiaosai Gan, Shirui Wu, Zhiying Chen, Wanjin Hu, Yanbing Wang, Ning Producer: 20120820 In: Neuroscience letters vol. 514 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A study on the Fermi resonance of phenol under the effects of pressure and temperature by Raman spectroscopy. [electronic resource] by Li, DongFei Hua, Zhong Liu, ChengZhi Fan, Cunbo Sun, ChengLin Li, ZuoWei Chen, WanJin Producer: 20180112 In: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy vol. 136 Pt C Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	ATP1A1 mutations cause intermediate Charcot-Marie-Tooth disease. [electronic resource] by He, Jin Guo, Lingling Lin, Shan Chen, Wenfeng Xu, Guorong Cai, Bin Xu, Liuqing Hong, Jingmei Qiu, Liangliang Wang, Ning Chen, Wanjin Producer: 20200504 In: Human mutation vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Dosage effect of multiple genes accounts for multisystem disorder of myotonic dystrophy type 1. [electronic resource] by Yin, Qi Wang, Hongye Li, Na Ding, Yifu Xie, Zhenfei Jin, Lifang Li, Yan Wang, Qiong Liu, Xinyi Xu, Liuqing Li, Qing Ma, Yongjian Cheng, Yanbo Wang, Kai Zhong, Cuiqing Yu, Qian Tang, Wei Chen, Wanjin Yang, Wenjun Zhang, Fan Ding, Chen Bao, Lan Zhou, Bin Hu, Ping Li, Jinsong Producer: 20210527 In: Cell research vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)