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

Year Number of Results
2004 1
2006 1
2007 1
2009 2
2010 5
2012 2
2013 1
2014 1
2016 3
2017 1
2018 3
2019 1
2020 1
2021 2
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2024 0

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PubMed (GeneRIF) for id: 805

26 results

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Page 1
Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative CALM1-3 Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death Victims.
Clemens DJ, Gray B, Bagnall RD, Tester DJ, Giudicessi JR, Maleszewski JJ, Crotti L, Schwartz PJ, Matthews E, Semsarian C, Behr ER, Ackerman MJ. Clemens DJ, et al. Circ Genom Precis Med. 2020 Dec;13(6):e003032. doi: 10.1161/CIRCGEN.120.003032. Epub 2020 Nov 15. Circ Genom Precis Med. 2020. PMID: 33191766 Free PMC article. No abstract available.
Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation.
Yamamoto Y, Makiyama T, Harita T, Sasaki K, Wuriyanghai Y, Hayano M, Nishiuchi S, Kohjitani H, Hirose S, Chen J, Yokoi F, Ishikawa T, Ohno S, Chonabayashi K, Motomura H, Yoshida Y, Horie M, Makita N, Kimura T. Yamamoto Y, et al. Hum Mol Genet. 2017 May 1;26(9):1670-1677. doi: 10.1093/hmg/ddx073. Hum Mol Genet. 2017. PMID: 28335032
26 results