Xinzhen Yin
4PUBLICATIONS
4CO-AUTHORS
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Publications (4)
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|Jul 07, 2022
Late-onset Pompe disease with a novel mutation and a rare phenotype: A case report.Xiaoli Si, Ruoxia Zhang, Shengqiang Yan
|Oct 21, 2021
Association analysis of SYT11, FGF20, GCH1 rare variants in Parkinson's disease.Jia-Li Pu, Zhi-Hao Lin, Ran Zheng
|Jul 16, 2020
A novel TFG c.793C>G mutation in a Chinese pedigree with Charcot-Marie-Tooth disease 2.Ding-Wen Wu, Yanfang Li, Xinzhen Yin
|Aug 15, 2018
Motor neuron disease-like phenotype associated with anti-IgLON5 disease.Qing-Qing Tao, Qiao Wei, Shui-Jiang Song
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