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Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.
Brain. 2022 Sep 14;145(9):2991-3009. doi: 10.1093/brain/awab321.
Brain. 2022.
PMID: 34431999
Free PMC article.
Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes.
Begemann A, Acuña MA, Zweier M, Vincent M, Steindl K, Bachmann-Gagescu R, Hackenberg A, Abela L, Plecko B, Kroell-Seger J, Baumer A, Yamakawa K, Inoue Y, Asadollahi R, Sticht H, Zeilhofer HU, Rauch A.
Begemann A, et al. Among authors: kroell seger j.
Mol Med. 2019 Feb 27;25(1):6. doi: 10.1186/s10020-019-0073-6.
Mol Med. 2019.
PMID: 30813884
Free PMC article.
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Infantile epileptic encephalopathy, transient choreoathetotic movements, and hypersomnia due to a De Novo missense mutation in the SCN2A gene.
Hackenberg A, Baumer A, Sticht H, Schmitt B, Kroell-Seger J, Wille D, Joset P, Papuc S, Rauch A, Plecko B.
Hackenberg A, et al. Among authors: kroell seger j.
Neuropediatrics. 2014 Aug;45(4):261-4. doi: 10.1055/s-0034-1372302. Epub 2014 Apr 7.
Neuropediatrics. 2014.
PMID: 24710820
Free article.
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The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study.
Papuc SM, Abela L, Steindl K, Begemann A, Simmons TL, Schmitt B, Zweier M, Oneda B, Socher E, Crowther LM, Wohlrab G, Gogoll L, Poms M, Seiler M, Papik M, Baldinger R, Baumer A, Asadollahi R, Kroell-Seger J, Schmid R, Iff T, Schmitt-Mechelke T, Otten K, Hackenberg A, Addor MC, Klein A, Azzarello-Burri S, Sticht H, Joset P, Plecko B, Rauch A.
Papuc SM, et al. Among authors: kroell seger j.
Eur J Hum Genet. 2019 Mar;27(3):408-421. doi: 10.1038/s41431-018-0299-8. Epub 2018 Dec 14.
Eur J Hum Genet. 2019.
PMID: 30552426
Free PMC article.
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