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Familial cohorts with early-onset epilepsy. A Identification of four missense mutations in the SETD1A gene. B Family pedigree of neonatal seizures and the p.R913C mutation in SETD1A. C–E Family pedigrees of the p.Q269R (C), p.G1369R (D), and p.R1392H (E) mutations in SETD1A.
