De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities.

2020
https://researcherprofiles.org/profile/88522630
31924697
Bina R, Matalon D, Fregeau B, Tarsitano JJ, Aukrust I, Houge G, Bend R, Warren H, Stevenson RE, Stuurman KE, Barkovich AJ, Sherr EH