Search Results - Yongxin Wen

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    Clinical and Genetic Heterogeneity in a Cohort of Chinese Children With Dopa-Responsive Dystonia by Yan Chen, Xinhua Bao, Yongxin Wen, Jiaping Wang, Qingping Zhang, Jiayou Yan

    Published 2020
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    Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation by Jiaping Wang, Qingping Zhang, Yan Chen, Shujie Yu, Xiru Wu, Xinhua Bao, Yongxin Wen

    Published 2018
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    CACNA1A Gene Variants in Eight Chinese Patients With a Wide Range of Phenotypes by Linxia Zhang, Linxia Zhang, Yongxin Wen, Qingping Zhang, Yan Chen, Jiaping Wang, Kaili Shi, Lijun Du, Xinhua Bao

    Published 2020
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