Jingshan Wu
2PUBLICATIONS
5CO-AUTHORS
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Publications (2)
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|Jan 22, 2021
Novel SPG4 Mutation in a Patient with Sporadic Hereditary Spastic Paraplegia and Elevated Cerebrospinal Fluid Protein.Hongda She, Xin Zheng, Yingxiu Xiao
|Dec 20, 2019
Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations.Wei Chen, Youqiao Zhang, Yifeng Ni
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