De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females

R. Webster, M. T. Cho, K. Retterer, F. Millan, C. Nowak, J. Douglas, A. Ahmad, G. V. Raymond, M. R. Johnson, A. Pujol, A. Begtrup, D. Mcknight, O. Devinsky, W. K. Chung

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