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. Author manuscript; available in PMC: 2016 Dec 1.
Published in final edited form as: Lancet Neurol. 2015 Sep 20;14(12):1219–1228. doi: 10.1016/S1474-4422(15)00199-4

Figure 1.

Figure 1

Estimated proportion of individuals with different types of epilepsy who carry a strong-acting, single mutation that either contributes substantially to or causes epilepsy.

Source: Kalachikov et al (2002),14 EuroEPINOMICS-RES Consortium, Epilepsy Phenome/Genome Project, Epi4k Consortium (2014),35 Epilepsy Phenome/Genome Project Epi4K Consortium (2015),57 Mefford et al (2011),58 Olson et al (2014),59 Dibbens et al (2013),60 Ishida et al (2013),61 Picard et al (2014),62 and Thomas et al (2014).63

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