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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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2013 | 1 |
2017 | 1 |
2018 | 1 |
2024 | 0 |
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Mutations in DEPDC5 cause familial focal epilepsy with variable foci.
Nat Genet. 2013 May;45(5):546-51. doi: 10.1038/ng.2599. Epub 2013 Mar 31.
Nat Genet. 2013.
PMID: 23542697
Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.
Tian WT, Huang XJ, Mao X, Liu Q, Liu XL, Zeng S, Guo XN, Shen JY, Xu YQ, Tang HD, Yin XM, Zhang M, Tang WG, Liu XR, Tang BS, Chen SD, Cao L.
Tian WT, et al.
Mov Disord. 2018 Mar;33(3):459-467. doi: 10.1002/mds.27274. Epub 2018 Jan 22.
Mov Disord. 2018.
PMID: 29356177
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ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsies.
Bennett CA, Petrovski S, Oliver KL, Berkovic SF.
Bennett CA, et al.
Neurol Genet. 2017 Jul 6;3(4):e163. doi: 10.1212/NXG.0000000000000163. eCollection 2017 Aug.
Neurol Genet. 2017.
PMID: 28717674
Free PMC article.
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