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Disrupted CaV1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model.
Kashiwa A, Makiyama T, Kohjitani H, Maurissen TL, Ishikawa T, Yamamoto Y, Wuriyanghai Y, Gao J, Huang H, Imamura T, Aizawa T, Nishikawa M, Chonabayashi K, Mishima H, Ohno S, Toyoda F, Sato S, Yoshiura KI, Takahashi K, Yoshida Y, Woltjen K, Horie M, Makita N, Kimura T. Kashiwa A, et al. Among authors: takahashi k. Heart Rhythm. 2023 Jan;20(1):89-99. doi: 10.1016/j.hrthm.2022.08.021. Epub 2022 Aug 23. Heart Rhythm. 2023. PMID: 36007726
Novel electrocardiographic criteria for short QT syndrome in children and adolescents.
Suzuki H, Horie M, Ozawa J, Sumitomo N, Ohno S, Hoshino K, Ehara E, Takahashi K, Maeda Y, Yoshinaga M, Tateno S, Takagi J, Doi S, Hoshina S, Sato I, Ishikawa T, Makita N, Chinushi M, Akazawa K, Nagashima M. Suzuki H, et al. Among authors: takahashi k. Europace. 2021 Dec 7;23(12):2029-2038. doi: 10.1093/europace/euab097. Europace. 2021. PMID: 34179980
SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families.
Wijeyeratne YD, Tanck MW, Mizusawa Y, Batchvarov V, Barc J, Crotti L, Bos JM, Tester DJ, Muir A, Veltmann C, Ohno S, Page SP, Galvin J, Tadros R, Muggenthaler M, Raju H, Denjoy I, Schott JJ, Gourraud JB, Skoric-Milosavljevic D, Nannenberg EA, Redon R, Papadakis M, Kyndt F, Dagradi F, Castelletti S, Torchio M, Meitinger T, Lichtner P, Ishikawa T, Wilde AAM, Takahashi K, Sharma S, Roden DM, Borggrefe MM, McKeown PP, Shimizu W, Horie M, Makita N, Aiba T, Ackerman MJ, Schwartz PJ, Probst V, Bezzina CR, Behr ER. Wijeyeratne YD, et al. Among authors: takahashi k. Circ Genom Precis Med. 2020 Dec;13(6):e002911. doi: 10.1161/CIRCGEN.120.002911. Epub 2020 Nov 9. Circ Genom Precis Med. 2020. PMID: 33164571 Free PMC article.
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