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HARVARD Citation
Webster, R. et al. (2017). De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females. Clinical genetics. 91 (5), pp. 756-763. [Online].
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Webster, R. et al. (2017). De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females. Clinical genetics. 91 (5), pp. 756-763. [Online].