De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities | Journal of Medical Genetics

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

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Cite this article as:: Bina R, Matalon D, Fregeau B, et al

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

Journal of Medical Genetics 2020;57:461-465.