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A de novo gain-of-function KCND3 mutation in early repolarization syndrome.
Takayama K, Ohno S, Ding WG, Ashihara T, Fukumoto D, Wada Y, Makiyama T, Kise H, Hoshiai M, Matsuura H, Horie M. Takayama K, et al. Among authors: fukumoto d. Heart Rhythm. 2019 Nov;16(11):1698-1706. doi: 10.1016/j.hrthm.2019.05.033. Epub 2019 Jun 4. Heart Rhythm. 2019. PMID: 31173922
Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote.
Fujii Y, Matsumoto Y, Hayashi K, Ding WG, Tomita Y, Fukumoto D, Wada Y, Ichikawa M, Sonoda K, Ozawa J, Makiyama T, Ohno S, Yamagishi M, Matsuura H, Horie M, Itoh H. Fujii Y, et al. Among authors: fukumoto d. J Cardiol. 2017 Jul;70(1):74-79. doi: 10.1016/j.jjcc.2016.09.010. Epub 2016 Nov 3. J Cardiol. 2017. PMID: 27816319 Free article.
63 results