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    Progressive myoclonic ataxia as an initial symptom of typical type I sialidosis with NEU1 mutation

    Progressive myoclonic ataxia as an initial symptom of typical type I sialidosis with NEU1 mutation by 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

    Published 2024-11-01
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    Article

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