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Shuqi Chen
Shuqi Chen
Zhejiang University
Medicine
Missense mutation
Genetics
SPTAN1
Paralysis
2
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SPTAN1 variants likely cause autosomal recessive complicated hereditary spastic paraplegia.
2021
Journal of Human Genetics
Fei Xie
Shuqi Chen
Peng Liu
Xinhui Chen
Wei Luo
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Six-Year Follow-Up of Dysphagia in Patients with Parkinson’s Disease
2021
Dysphagia
Ping Wang
Bo Wang
Xinhui Chen
Bing Xiong
Fangyao Xie
Sheng Wu
Yinshan Tang
Shuqi Chen
Xueping Ding
Peng Liu
Wei Luo
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