Huan Hu

KIF11 mutations are a common cause of autosomal dominant familial exudative vitreoretinopathy

Xueshan Xiao, Shi-qiang Li, Qingjiong Zhang, 2015, British Journal of Ophthalmology.

KIF11 mutations are a common cause of autosomal dominant familial exudative vitreoretinopathy

Xueshan Xiao, Shi-qiang Li, Qingjiong Zhang, 2015, British Journal of Ophthalmology.

Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients

Kun Sun, Sun Chen, Bing Zhang, 2023, Frontiers in Genetics.

Novel BEST1 mutations and special clinical characteristics of autosomal recessive bestrophinopathy in Chinese patients

Mingkai Lin, Xing Liu, Hui Xiao, 2018, Acta ophthalmologica.

Driver mutations in ADGRL3 are involved in the evolution of ependymoma

J. Zeng, Zhi Li, Y. Xia, 2022, Laboratory Investigation.