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Oates, Stephanie; Absoud, Michael; Goyal, Sushma; Bayley, Sophie; Baulcomb, Jennifer; Sims, Annemarie; Riddett, Amy; Allis, Katrina; Brasch-Andersen, Charlotte; Balasubramanian, Meena; Bai, Renkui; Callewaert, Bert; Hüffmeier, Ulrike; Le Duc, Diana; Radtke, Maximilian; Korff, Christian; Kennedy, Joanna; Low, Karen; Møller, Rikke S; Nielsen, Jens Erik Klint; ... (2021). ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder. Clinical genetics, 100(4), pp. 412-429. Wiley-Blackwell 10.1111/cge.14023
Ranza, Emmanuelle; Z'Graggen, Werner; Lidgren, Mathias; Beghetti, Maurice; Guipponi, Michel; Antonarakis, Stylianos E; Absoud, Michael; Goyal, Sushma; Pal, Deb K; Korff, Christian M (2020). SCN8A heterozygous variants are associated with anoxic-epileptic seizures. American journal of medical genetics. Part A, 182(5), pp. 1209-1216. Wiley 10.1002/ajmg.a.61513
