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Non-missense variants of KCNH2 show better outcomes in type 2 long QT syndrome.
Aizawa T, Wada Y, Hasegawa K, Huang H, Imamura T, Gao J, Kashiwa A, Kohjitani H, Fukuyama M, Kato K, Kato ET, Hisamatsu T, Ohno S, Makiyama T, Kimura T, Horie M. Aizawa T, et al. Among authors: fukuyama m. Europace. 2023 Apr 15;25(4):1491-1499. doi: 10.1093/europace/euac269. Europace. 2023. PMID: 36861347 Free PMC article.
A Common Mutation of Long QT Syndrome Type 1 in Japan.
Itoh H, Dochi K, Shimizu W, Denjoy I, Ohno S, Aiba T, Kimura H, Kato K, Fukuyama M, Hasagawa K, Schulze-Bahr E, Guicheney P, Horie M. Itoh H, et al. Among authors: fukuyama m. Circ J. 2015;79(9):2026-30. doi: 10.1253/circj.CJ-15-0342. Epub 2015 Jun 29. Circ J. 2015. PMID: 26118460 Free article. Clinical Trial.
Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family.
Ichikawa M, Ohno S, Fujii Y, Ozawa J, Sonoda K, Fukuyama M, Kato K, Kimura H, Itoh H, Hayashi H, Horie M. Ichikawa M, et al. Among authors: fukuyama m. Intern Med. 2016;55(3):259-62. doi: 10.2169/internalmedicine.55.6014. Epub 2016 Feb 1. Intern Med. 2016. PMID: 26831020 Free article.
302 results