Soldovieri MV et al. (2014). Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A. Human mutation. 35 [PubMed]

See more from authors: Soldovieri MV · Boutry-Kryza N · Milh M · Doummar D · Heron B · Bourel E · Ambrosino P · Miceli F · De Maria M · Dorison N · Auvin S · Echenne B · Oertel J · Riquet A · Lambert L · Gerard M · Roubergue A · Calender A · Mignot C · Taglialatela M · Lesca G

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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