DOI: 10.1055/s-00029025

Journal of Pediatric Epilepsy

References

Syrbe S, Hedrich UB, Riesch E , et al; EuroEPINOMICS RES.
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.

Nat Genet 2015;
47 (4) 393-399

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