Xin Li

A novel missense NMNAT1 mutation identified in a consanguineous family with Leber congenital amaurosis by targeted next generation sequencing.

X. Yi, Yan-ping Wang, Jun Zhu, 2015, Gene.

Systematic evaluation of a targeted gene capture sequencing panel for molecular diagnosis of retinitis pigmentosa

Asan, X. Yi, Xiuqing Zhang, 2018, PloS one.

Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing

M. Qi, Yuehong Yang, Yue Yang, 2014, Journal of Zhejiang University-SCIENCE B.

Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing

M. Qi, Yuehong Yang, Hui Huang, 2014, Journal of Zhejiang University-SCIENCE B.