Hongyan Li

WDR73 Depletion Destabilizes PIP4K2C Activity and Impairs Focal Adhesion Formation in Galloway–Mowat Syndrome

D. Liang, Zhuo Li, Lingqian Wu, 2022, Biology.

Novel GZF1 pathogenic variants identified in two Chinese patients with Larsen syndrome

D. Liang, Zhuo Li, Lingqian Wu, 2020, Clinical genetics.

Five novel mutations of the FRMD7 gene in Chinese families with X-linked infantile nystagmus

Kanxing Zhao, J. Hejtmancik, Liming Wang, 2008, Molecular vision.

Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosis

D. Liang, Zhuo Li, Lingqian Wu, 2021, Human Genetics.

Five novel mutations of the FRMD7 gene in Chinese families with X-linked infantile nystagmus

Kanxing Zhao, J. Hejtmancik, Liming Wang, 2008, Molecular vision.