Xiangdong Kong

4PUBLICATIONS
0CO-AUTHORS
Pacific Peoples and disabilityGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseases
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (4)

|Apr 12, 2024
Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients.

Xuechao Zhao, Haofeng Ning, Lina Liu

|Feb 26, 2022
Genetic analysis and identification of novel variations in Chinese patients with pediatric epilepsy by whole-exome sequencing.

Xuechao Zhao, Haofeng Ning, Yanhong Wang

|Apr 22, 2020
A novel PCDH19 missense mutation, c.812G>A (p.Gly271Asp), identified using whole-exome sequencing in a Chinese family with epilepsy female restricted mental retardation syndrome.

Xuechao Zhao, Yanhong Wang, Shiyue Mei

|Apr 11, 2019
Novel mutations of COL4A3, COL4A4, and COL4A5 genes in Chinese patients with Alport Syndrome using next generation sequence technique.

Xuechao Zhao, Chen Chen, Yanfu Wei

Pageof 1

Frequent Collaborators