De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities.
Bina R, Matalon D, Fregeau B, Tarsitano JJ, Aukrust I, Houge G, Bend R, Warren H, Stevenson RE, Stuurman KE, Barkovich AJ, Sherr EH.
Bina R, et al. Among authors: tarsitano jj.
J Med Genet. 2020 Jul;57(7):461-465. doi: 10.1136/jmedgenet-2019-106193. Epub 2020 Jan 10.
J Med Genet. 2020.
PMID: 31924697
Free PMC article.