Two Novel Variants of WDR26 in Chinese Patients with Intellectual Disability

Hu, JC; Xu, MM; Zhu, XB; Zhang, Y

Zhang, Y (通讯作者),Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Neurol, Shanghai 200092, Peoples R China.

GENES, 2022; 13 (5):

Abstract

Skraban-Deardorff syndrome is a rare autosomal dominant genetic disease caused by variants in the WDR26 gene. Here, we report two Chinese patients dia......

Full Text Link