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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
Research output: Contribution to journal › Article › peer-review
23
Scopus
citations