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Comment
. 2025 Apr 30;25(3):158-160.
doi: 10.1177/15357597251333279. eCollection 2025 May-Jun.

From All to One: Can a Large Cohort of Individuals with SCN1A-Related Epilepsy Offer Predictions for Other Individuals With SCN1A Variants?

Elizabeth E Gerard  1
Affiliations
Comment

From All to One: Can a Large Cohort of Individuals with SCN1A-Related Epilepsy Offer Predictions for Other Individuals With SCN1A Variants?

Elizabeth E Gerard. Epilepsy Curr. .
No abstract available

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Comment on

  • Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsies.
    Gallagher D, Pérez-Palma E, Bruenger T, Ghanty I, Brilstra E, Ceulemans B, Chemaly N, de Lange I, Depienne C, Guerrini R, Mei D, Møller RS, Nabbout R, Regan BM, Schneider AL, Scheffer IE, Schoonjans AS, Symonds JD, Weckhuysen S, Zuberi SM, Lal D, Brunklaus A. Gallagher D, et al. Epilepsia. 2024 Apr;65(4):1046-1059. doi: 10.1111/epi.17882. Epub 2024 Feb 27. Epilepsia. 2024. PMID: 38410936

References

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    1. Gallagher D, Pérez-Palma E, Bruenger Tet al. Genotype–phenotype associations in 1018 individuals with SCN1A-related epilepsies. Epilepsia. 2024;65(4):1046–1059. doi: 10.1111/epi.17882 - DOI - PubMed
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    1. Guerrini R, Cellini E, Mei Det al. et al. Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene. Epilepsia. 2010;51(12):2474–2477. doi: 10.1111/j.1528-1167.2010.02790.x - DOI - PubMed

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