Genetic analysis of a family with skeletal muscle ion channelopathy and hereditary spastic paraplegia type 7 caused by SCN4A and SPG7 double mutations

作者：Hongping Yu, Ziyan Xu, Maoxiong Wu, Qian Chen, Zhihai Zheng, Wei Wen, Pan Lin, Jing Zou, Jianhui Zhang, Dan‐dan Ruan, Dan-dan Ruan, Ruo-li Wang, Ruo-li Wang, Li Chen, Mei-zhu Gao, Li Zhang, Congjun Li, Fan Lin, Hong Li, Zhu-ting Fang, Wei Wang, Xing-lin Ruan, Jie-wei Luo, Yunfei Li · 发表于：Gene · 年份：2025 · DOI：10.1016/j.gene.2025.149782 · 研究领域：Hereditary Neurological Disorders、Neurological diseases and metabolism、Neurogenetic and Muscular Disorders Research