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Comment

. 2012 Dec;8(12):658.

doi: 10.1038/nrneurol.2012.229. Epub 2012 Nov 13.

Genetics: mutations in potassium channel KCNT1-a novel driver of epilepsy pathogenesis

PMID: 23147853
DOI: 10.1038/nrneurol.2012.229

Comment

Genetics: mutations in potassium channel KCNT1-a novel driver of epilepsy pathogenesis

Katie Kingwell. Nat Rev Neurol. 2012 Dec.

. 2012 Dec;8(12):658.

doi: 10.1038/nrneurol.2012.229. Epub 2012 Nov 13.

Author

PMID: 23147853
DOI: 10.1038/nrneurol.2012.229

No abstract available

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Comment on

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy.
Heron SE, Smith KR, Bahlo M, Nobili L, Kahana E, Licchetta L, Oliver KL, Mazarib A, Afawi Z, Korczyn A, Plazzi G, Petrou S, Berkovic SF, Scheffer IE, Dibbens LM. Heron SE, et al. Nat Genet. 2012 Nov;44(11):1188-90. doi: 10.1038/ng.2440. Epub 2012 Oct 21. Nat Genet. 2012. PMID: 23086396

References

1. Nat Genet. 2012 Nov;44(11):1188-90 - PubMed
1. Nat Genet. 2012 Nov;44(11):1255-9 - PubMed

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