Ru Shen
3PUBLICATIONS
14CO-AUTHORS
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Publications (3)
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|Sep 03, 2025
Clinical and Genetic Functional Validation of a Novel AP1S1 Mutation Causing MEDNIK Syndrome.Lifen Duan, Ru Shen, Guoyan Yin
|Mar 17, 2021
A novel TUBG1 mutation with neurodevelopmental disorder caused by malformations of cortical development.Ru Shen, Zhen Zhang, Yu Zhuang
|Feb 25, 2021
A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype.Lulu Yan, Ru Shen, Zongfu Cao
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