Search Results - Xujun Chu

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  1. 1

    A novel KIDINS220 mutation associated with hereditary spastic paraplegia accompanied by severe peripheral neuropathy by Xujun Chu, Jin Xu, Yilei Zheng, Xiaoyu Liu, Yun Yuan, Rui Wu

    Published in Frontiers in Neuroscience (2025-10-01)
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  2. 2

    A novel variant of biallelic MME gene associated with autosomal recessive late-onset distal hereditary motor neuropathy in Chinese families by Bentuo Zhang, Qiang Gang, Lingchao Meng, Zhenyu Li, Xujun Chu, Haohao Wu, Junsu Yang, Baogang Huang, Kang Du

    Published in BMC Medical Genomics (2024-09-01)
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  3. 3

    Skeletal Muscle Involvement Pattern of Hereditary Transthyretin Amyloidosis: A Study Based on Muscle MRI by Xujun Chu, Kang Du, Yuwei Tang, Xutong Zhao, Meng Yu, Yiming Zheng, Jianwen Deng, He Lv, Wei Zhang, Zhaoxia Wang, Yun Yuan, Yun Yuan, Lingchao Meng, Lingchao Meng

    Published in Frontiers in Neurology (2022-05-01)
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  4. 4

    First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-Sarcoglycanopathy by Zhiying Xie, Chengyue Sun, Chang Liu, Xujun Chu, Qiang Gang, Meng Yu, Yiming Zheng, Lingchao Meng, Fan Li, Dongliang Xia, Li Wang, Ying Li, Jianwen Deng, He Lv, Zhaoxia Wang, Wei Zhang, Yun Yuan

    Published in Frontiers in Pediatrics (2022-06-01)
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  5. 5

    Clinical and biochemical characterization of hereditary transthyretin amyloidosis caused by E61K mutation by Xujun Chu, Mengdie Wang, Mengdie Wang, Ran Tang, Yanan Huang, Jiaxi Yu, Yunfeng Cao, Yilei Zheng, Zhiying Xie, Jianwen Deng, Zhi Wang, Wei Ma, Wenjing Song, Yuan Wu, He Lv, Wei Zhang, Zhaoxia Wang, Yun Yuan, Yu Liu, Lingchao Meng

    Published in Frontiers in Molecular Neuroscience (2022-10-01)
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