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J-GLOBAL ID:201502214922754691   Reference number:15A0871482

Association Between Genetic Variation in the SCN10A Gene and Cardiac Conduction Abnormalities in Patients With Hypertrophic Cardiomyopathy

肥大型心筋症患者におけるSCN10A遺伝子の遺伝子変異と心伝導異常との関連
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Volume: 56  Issue:Page: 421-427 (J-STAGE)  Publication year: 2015 
JST Material Number: Z0752A  ISSN: 1349-2365  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: ENGLISH (EN)
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Cardiovascular system diseases 
Reference (36):
  • 1. Maron BJ, Gardin JM, Flack JM, Gidding SS, Kurosaki TT, Bild DE. Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults. Circulation 1995; 92: 785-9.
  • 2. Maron BJ, Maron MS. Hypertrophic cardiomyopathy. Lancet 2013; 381: 242-55.
  • 3. Otsuka H, Arimura T, Abe T, et al. Prevalence and distribution of sarcomeric gene mutations in Japanese patients with familial hypertrophic cardiomyopathy. Circ J 2012; 76: 453-61.
  • 4. Kubo T, Kitaoka H, Okawa M, et al. Genetic screening and double mutation in Japanese patients with hypertrophic cardiomyopathy. Circ J 2011; 75: 2654-9.
  • 5. Ogimoto A, Okayama H, Nagai T, et al. Impact of synergistic polymorphisms in adrenergic receptor-related genes and cardiovascular events in patients with dilated cardiomyopathy. Circ J 2012; 76: 2003-8.
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