De novo variants inSUPT16Hcause neurodevelopmental disorders associated with corpus callosum abnormalities

R Bina, D Matalon, B Fregeau, JJ Tarsitano, I Aukrust, G Houge, R Bend, H Warren, RE Stevenson, Kyra Stuurman, AJ Barkovich, EH Sherr

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)461-465
Number of pages5
JournalJournal of Medical Genetics
Issue number7
Publication statusPublished - 2020

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