Yingchun Zheng

3PUBLICATIONS
2CO-AUTHORS
Gene and molecular therapyNeurology and neuromuscular diseasesCrystallography
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Publications (3)

|Jun 06, 2023
The loss of function GBA1 c.231C > G mutation associated with Parkinson disease.

Dejie Chen, Yingchun Zheng, Guilian Zhang

|Oct 03, 2020
The gain-of-function FAM83H mutation caused hypocalcification amelogenesis imperfecta in a Chinese family.

Yingchun Zheng, Ting Lu, Jianfan Chen

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