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Results by year

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

Year Number of Results
1997 1
2001 1
2002 3
2003 2
2005 3
2006 3
2007 2
2008 6
2009 3
2010 4
2011 6
2012 7
2013 4
2014 4
2015 6
2016 6
2017 8
2018 6
2019 9
2020 7
2021 11
2022 16
2023 2
2024 0

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Similar articles for PMID: 36252966

103 results

Results by year

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Page 1
De novo loss-of-function KCNMA1 variants are associated with a new multiple malformation syndrome and a broad spectrum of developmental and neurological phenotypes.
Liang L, Li X, Moutton S, Schrier Vergano SA, Cogné B, Saint-Martin A, Hurst ACE, Hu Y, Bodamer O, Thevenon J, Hung CY, Isidor B, Gerard B, Rega A, Nambot S, Lehalle D, Duffourd Y, Thauvin-Robinet C, Faivre L, Bézieau S, Dure LS, Helbling DC, Bick D, Xu C, Chen Q, Mancini GMS, Vitobello A, Wang QK. Liang L, et al. Hum Mol Genet. 2019 Sep 1;28(17):2937-2951. doi: 10.1093/hmg/ddz117. Hum Mol Genet. 2019. PMID: 31152168 Free PMC article.
KCNMA1-linked channelopathy.
Bailey CS, Moldenhauer HJ, Park SM, Keros S, Meredith AL. Bailey CS, et al. J Gen Physiol. 2019 Oct 7;151(10):1173-1189. doi: 10.1085/jgp.201912457. Epub 2019 Aug 19. J Gen Physiol. 2019. PMID: 31427379 Free PMC article. Review.
103 results