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

Autor: Lin, Jingjing1 (AUTHOR), Li, Yun‐Lu1 (AUTHOR), Chen, Bo‐Li1 (AUTHOR), Su, Hui‐Zhen1 (AUTHOR), Zeng, Yi‐Heng1 (AUTHOR), Zeng, Rui‐Huang1 (AUTHOR), Zhang, Yu‐Duo1 (AUTHOR), Chen, Ru‐Kai1 (AUTHOR), Cai, Nai‐Qing1 (AUTHOR), Chen, Yi‐Kun1 (AUTHOR), Yuan, Ru‐Ying1 (AUTHOR), Jiang, Jun‐Yi1 (AUTHOR), Yao, Xiang‐Ping1 (AUTHOR), Wang, Ning1 (AUTHOR), Chen, Wan‐Jin1 (AUTHOR) wanjinchen75@fjmu.edu.cn, Yang, Kang1 (AUTHOR) ykang319@fjmu.edu.cn
Zdroj: Annals of Clinical & Translational Neurology. Nov2024, Vol. 11 Issue 11, p2998-3009. 12p.
Databáze: Academic Search Ultimate
Nepřihlášeným uživatelům se plný text nezobrazuje