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	1.	[Detection for trinucleotide repeats in myotonic dystrophy type 1]. [electronic resource] by Li, Yun Da, Yu-wei Producer: 20120710 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[A study of vascular factor in the pathogenesis of polymyositis]. [electronic resource] by Wang, Min Jia, Jian-ping Da, Yu-wei Producer: 20050902 In: Zhonghua nei ke za zhi vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Clinical and imaging features and genetic analysis of a case with adult-onset Krabbe disease]. [electronic resource] by Da, Yu-wei Li, Yun Zhang, Xin-qing Jia, Jian-ping Producer: 20140102 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Giant axonal neuropathy caused by a novel compound heterozygous mutation in the gigaxonin gene. [electronic resource] by Xu, Min Da, Yu-wei Liu, Lu Wang, Fen Jia, Jian-ping Producer: 20140507 In: Journal of child neurology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	An unusual case with myotonia. [electronic resource] by Da, Yu-Wei Wang, Min Li, Yun Lu, Yan Jia, Jian-Ping Producer: 20131126 In: The Kaohsiung journal of medical sciences vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis. [electronic resource] by Lu, Yan Da, Yu-Wei Zhang, Yong-Biao Li, Xin-Gang Wang, Min Di, Li Pang, Mi Lei, Lin Publication details: Frontiers in neuroscience 2018 In: Frontiers in neuroscience vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis. [electronic resource] by Lu, Yan Da, Yu-Wei Zhang, Yong-Biao Li, Xin-Gang Wang, Min Di, Li Pang, Mi Lei, Lin Publication details: Frontiers in neuroscience 2018 In: Frontiers in neuroscience vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Pathological Observation of Blood Stasis Syndrome in Non-diabetic Peripheral Neuropathies: A Retrospective Analysis Based on Nerve Biopsy. [electronic resource] by Xu, Min Chen, Hai Shi, Zai-Xiang Da, Yu-Wei Luo, Yu-Min Gao, Li Lu, Yan Wang, Min Di, Li Producer: 20210702 In: Chinese journal of integrative medicine vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Presence of antibodies against low-density lipoprotein receptor-related protein 4 and impairment of neuromuscular junction in a Chinese cohort of amyotrophic lateral sclerosis. [electronic resource] by Lei, Lin Shen, Xin-Ming Wang, Shu-Yan Lu, Yan Wang, Suo-Bin Chen, Hai Liu, Zheng Ouyang, Ya-Sheng Duo, Jian-Ying Da, Yu-Wei Chen, Zhi-Guo Producer: 20191216 In: Chinese medical journal vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)