Search Results - Xingzhi Chang

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    Clinical and genetic analysis of a case with centronuclear myopathy caused by SPEG gene mutation: a case report and literature review by Gang Zhang, Min Xu, Tingting Huang, Wenxin Lin, Jinglin Chen, Wangyang Chen, Xingzhi Chang

    Published 2021
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    Clinical and genetic features of infancy-onset congenital myopathies from a Chinese paediatric centre by Yu Zhang, Hui Yan, Jieyu Liu, Huifang Yan, Yinan Ma, Cuijie Wei, Zhaoxia Wang, Hui Xiong, Xingzhi Chang

    Published 2022
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    A 1-year analysis from a natural history study in Chinese individuals with Duchenne muscular dystrophyResearch in context by Xihua Li, Junlan Lv, Wenhua Zhu, Siqi Hong, Zhiqiang Wang, Xingzhi Chang, Ying Xu Gao, Yangmei Zhou, Caiping Jia, Jia Fang, Terrell A. Patterson

    Published 2024
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