Kun Xia
4PUBLICATIONS
4CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (4)
Sort by Publication Date:
|Jan 15, 2020
A founder RDH5 splice site mutation leads to retinitis punctata albescens in two inbred Pakistani kindreds.Rizwan Khan, Rana Muhammad Kamran Shabbir, Irum Raza
|Dec 12, 2018
Genotype and phenotype correlations for SHANK3 de novo mutations in neurodevelopmental disorders.Ying Li, Xiangbin Jia, Huidan Wu
|Sep 27, 2017
Not all neuroligin 3 and 4X missense variants lead to significant functional inactivation.Xiaojuan Xu, Zhengmao Hu, Lusi Zhang
|Apr 14, 2017
Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder.Jinchen Li, Lin Wang, Ping Yu
Pageof 1
