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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1998 | 2 |
2009 | 1 |
2024 | 0 |
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A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
PLoS Genet. 2009 Sep;5(9):e1000649. doi: 10.1371/journal.pgen.1000649. Epub 2009 Sep 18.
PLoS Genet. 2009.
PMID: 19763161
Free PMC article.
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M.
Charlier C, et al.
Nat Genet. 1998 Jan;18(1):53-5. doi: 10.1038/ng0198-53.
Nat Genet. 1998.
PMID: 9425900
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A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.
Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, Ronen GM, Bjerre I, Quattlebaum T, Murphy JV, McHarg ML, Gagnon D, Rosales TO, Peiffer A, Anderson VE, Leppert M.
Singh NA, et al.
Nat Genet. 1998 Jan;18(1):25-9. doi: 10.1038/ng0198-25.
Nat Genet. 1998.
PMID: 9425895
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