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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 1 |
2020 | 1 |
2022 | 1 |
2024 | 0 |
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Stichodactyla helianthus peptide, a pharmacological tool for studying Kv3.2 channels.
Mol Pharmacol. 2005 May;67(5):1513-21. doi: 10.1124/mol.105.011064. Epub 2005 Feb 11.
Mol Pharmacol. 2005.
PMID: 15709110
Whole-Exome Sequencing in NF1-Related West Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy.
Rademacher A, Schwarz N, Seiffert S, Pendziwiat M, Rohr A, van Baalen A, Helbig I, Weber Y, Muhle H.
Rademacher A, et al.
Neuropediatrics. 2020 Oct;51(5):368-372. doi: 10.1055/s-0040-1710524. Epub 2020 May 11.
Neuropediatrics. 2020.
PMID: 32392612
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Emerging evidence of genotype-phenotype associations of developmental and epileptic encephalopathy due to KCNC2 mutation: Identification of novel R405G.
Wang S, Yu Y, Wang X, Deng X, Ma J, Liu Z, Gu W, Sun D.
Wang S, et al.
Front Mol Neurosci. 2022 Aug 25;15:950255. doi: 10.3389/fnmol.2022.950255. eCollection 2022.
Front Mol Neurosci. 2022.
PMID: 36090251
Free PMC article.
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