Carvill GL et al. (2013). Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1. Nature genetics. 45 [PubMed]

See more from authors: Carvill GL · Heavin SB · Yendle SC · McMahon JM · O'Roak BJ · Cook J · Khan A · Dorschner MO · Weaver M · Calvert S · Malone S · Wallace G · Stanley T · Bye AM · Bleasel A · Howell KB · Kivity S · Mackay MT · Rodriguez-Casero V · Webster R · Korczyn A · Afawi Z · Zelnick N · Lerman-Sagie T · Lev D · Møller RS · Gill D · Andrade DM · Freeman JL · Sadleir LG · Shendure J · Berkovic SF · Scheffer IE · Mefford HC

References and models cited by this paper
References and models that cite this paper

Miceli F et al. (2015). Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits. The Journal of neuroscience : the official journal of the Society for Neuroscience. 35 [PubMed]

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