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Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

, , , , , , , , , , , , , , , , , and . Human Genetics and Genomics Advances, 3 (4): 100131 (2022)
DOI: https://doi.org/10.1016/j.xhgg.2022.100131

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