Hasil Pencarian - En-Lin Dong

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  1. 1
    Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76)

    Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mu... oleh Ying-qian Lu, En-lin Dong, Wei-qi Yang, Lu-lu Lai, Xiao-hong Lin, Li-xiang Ma, Wan-jin Chen, Ning Wang, Xiang Lin

    Diterbitkan 2019-01-01
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  2. 2
    Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia

    Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia oleh Lu‐Lu Lai, Yi‐Jun Chen, Yun‐Lu Li, Xiao‐Hong Lin, Meng‐Wen Wang, En‐Lin Dong, Ning Wang, Wan‐Jin Chen, Xiang Lin

    Diterbitkan 2020-10-01
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  3. 3
    Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China

    Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China oleh En-Lin Dong, Chong Wang, Shuang Wu, Ying-Qian Lu, Xiao-Hong Lin, Hui-Zhen Su, Miao Zhao, Jin He, Li-Xiang Ma, Ning Wang, Wan-Jin Chen, Xiang Lin

    Diterbitkan 2018-07-01
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  4. 4
    Novel Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia

    Novel Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia oleh Yi-Jun Chen, Zai-Qiang Zhang, Meng-Wen Wang, Yu-Sen Qiu, Ru-Ying Yuan, En-Lin Dong, Zhe Zhao, Hai-Tao Zhou, Ning Wang, Ning Wang, Wan-Jin Chen, Wan-Jin Chen, Xiang Lin, Xiang Lin

    Diterbitkan 2021-05-01
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