S. Luo

Rare NRXN1 missense variants identified in autism interfered protein degradation and Drosophila sleeping.

K. Xia, L. Xia, Lu Shen, 2021, Journal of psychiatric research.

Exome sequencing identifies UPF3B as the causative gene for a Chinese non‐syndrome mental retardation pedigree

Y. Zheng, K. Xia, Z. Xiong, 2013, Clinical genetics.

GLA variation p.E66Q identified as the genetic etiology of Fabry disease using exome sequencing.

K. Xia, Hui Guo, Zhengmao Hu, 2016, Gene.

Novel FLG mutations associated with ichthyosis vulgaris in the Chinese population

K. Xia, Z. Xiong, L. Zhang, 2012, Clinical and experimental dermatology.

CRISPR/Cas9-Mediated in vivo Genetic Correction in a Mouse Model of Hemophilia A

D. Liang, Wenzhou Li, Yong Wu, 2021, Frontiers in Cell and Developmental Biology.

Association of genetic variants of GRIN2B with autism

Jingping Zhao, K. Xia, Z. Xiong, 2015, Scientific Reports.

Hutchinson-Gilford progeria syndrome accompanied by severe skeletal abnormalities in two Chinese siblings: two case reports

K. Xia, Z. Xiong, Zhengmao Hu, 2013, Journal of Medical Case Reports.