Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome

 

Deletion of KDM6A"We report KDM6A mutations as a cause of KS in one male and two females. Our findings confirm both KS genetic heterogeneity and a locus on the X chromosome, as has been suggested previously."
Files: 
Support KSN -- Donate now

User login

Languages