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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 1
2000 4
2001 3
2002 2
2003 3
2004 2
2005 2
2006 3
2007 2
2009 2
2011 2
2012 2
2013 3
2014 2
2015 1
2016 5
2017 4
2018 2
2019 1
2020 4
2021 1
2022 1
2023 4
2024 0

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PubMed for id: 3781

46 results

Results by year

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Page 1
Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders.
Mochel F, Rastetter A, Ceulemans B, Platzer K, Yang S, Shinde DN, Helbig KL, Lopergolo D, Mari F, Renieri A, Benetti E, Canitano R, Waisfisz Q, Plomp AS, Huisman SA, Wilson GN, Cathey SS, Louie RJ, Gaudio DD, Waggoner D, Kacker S, Nugent KM, Roeder ER, Bruel AL, Thevenon J, Ehmke N, Horn D, Holtgrewe M, Kaiser FJ, Kamphausen SB, Abou Jamra R, Weckhuysen S, Dalle C, Depienne C. Mochel F, et al. Brain. 2020 Dec 1;143(12):3564-3573. doi: 10.1093/brain/awaa346. Brain. 2020. PMID: 33242881
KCNN2 polymorphisms and cardiac tachyarrhythmias.
Yu CC, Chia-Ti T, Chen PL, Wu CK, Chiu FC, Chiang FT, Chen PS, Chen CL, Lin LY, Juang JM, Ho LT, Lai LP, Yang WS, Lin JL. Yu CC, et al. Medicine (Baltimore). 2016 Jul;95(29):e4312. doi: 10.1097/MD.0000000000004312. Medicine (Baltimore). 2016. PMID: 27442679 Free PMC article.
46 results