অনুসন্ধান ফলাফলগুলি - Xingzhi Chang

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

Connect to this object online.

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

Connect to this object online.

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

Connect to this object online.