Progressive myoclonic ataxia as an initial symptom of typical type I sialidosis with NEU1 mutation
进行性肌阵挛性共济失调是 NEU1 突变典型 I 型唾液酸沉积症的首发症状
期刊:Annals of Clinical and Translational Neurology
影响因子:4.4
doi:10.1002/acn3.52212
Jingjing Lin #, Yun-Lu Li #, Bo-Li Chen #, Hui-Zhen Su, Yi-Heng Zeng, Rui-Huang Zeng, Yu-Duo Zhang, Ru-Kai Chen, Nai-Qing Cai, Yi-Kun Chen, Ru-Ying Yuan, Jun-Yi Jiang, Xiang-Ping Yao, Ning Wang, Wan-Jin Chen, Kang Yang
