The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy by Feng Lin, Kang Yang, Min‐ting Lin, Fu‐ze Zheng, Long Chen, Yuan‐liang Ding, Zhi‐xian Ye, Xin Lin, Ning Wang, Zhi‐qiang Wang

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Dysferlinopathy in a cohort of Chinese patients: clinical features, mutation spectrum, and imaging findings by Qi-Fu Guo, Zhi-Xian Ye, Liang-Liang Qiu, Xin Lin, Jia-He Lai, Min-Ting Lin, Zhi-Qiang Wang, Ning Wang, Feng Lin, Jing Ni

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Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients by Feng Lin, Kang Yang, Xin Lin, Ming Jin, Long Chen, Fu-ze Zheng, Liang-liang Qiu, Zhi-xian Ye, Hai-zhu Chen, Min-ting Lin, Ning Wang, Zhi-qiang Wang

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Altered brain white matter structural motor network in spinocerebellar ataxia type 3 by Xin‐Yuan Chen, Zi‐Qiang Huang, Wei Lin, Meng‐Cheng Li, Zhi‐Xian Ye, Yu‐Sen Qiu, Xiao‐Yue Xia, Na‐Ping Chen, Jian‐Ping Hu, Shi‐Rui Gan, Qun‐Lin Chen

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Associations between CAG repeat size, brain and spinal cord volume loss, and motor symptoms in spinocerebellar ataxia type 3: a cohort study by Zhi-Xian Ye, Xuan-Yu Chen, Meng-Cheng Li, Xin-Yuan Chen, Yu-Sen Qiu, Ru-Ying Yuan, Zhi-Li Chen, Min-Ting Lin, Jian-Ping Hu, Ying Fu, Wan-Jin Chen, Ning Wang, Shi-Rui Gan, on behalf of the OSCCAR Investigators

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A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2 by Liang-Liang Qiu, Xiao-Dan Lin, Guo-Rong Xu, Li-Li Wang, Zhi-Xian Ye, Feng Lin, Hai-Zhu Chen, Min-Ting Lin, Nai-Qing Cai, Ming Jin, Liu-Qing Xu, Wei Hu, Ning Wang, Zhi-Qiang Wang, Li-Shao Guo

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Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort study by Xiang Lin, Ying Liu, Yi Lin, Ning Wang, Wan-Jin Chen, Ying Fu, Xiao-Hong Lin, Yu-Sen Qiu, Yi-Heng Zeng, Ru-Ying Yuan, Zhi-Xian Ye, Jin Bi, Yi-Jun Chen, Meng-Wen Wang, Shao-Bo Yao, Yi-Kun Chen, Jun-Yi Jiang

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