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Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseases.
Hayashi K, Teramoto R, Nomura A, Asano Y, Beerens M, Kurata Y, Kobayashi I, Fujino N, Furusho H, Sakata K, Onoue K, Chiang DY, Kiviniemi TO, Buys E, Sips P, Burch ML, Zhao Y, Kelly AE, Namura M, Kita Y, Tsuchiya T, Kaku B, Oe K, Takeda Y, Konno T, Inoue M, Fujita T, Kato T, Funada A, Tada H, Hodatsu A, Nakanishi C, Sakamoto Y, Tsuda T, Nagata Y, Tanaka Y, Okada H, Usuda K, Cui S, Saito Y, MacRae CA, Takashima S, Yamagishi M, Kawashiri MA, Takamura M. Hayashi K, et al. Among authors: hodatsu a. Cardiovasc Res. 2020 Nov 1;116(13):2116-2130. doi: 10.1093/cvr/cvaa010. Cardiovasc Res. 2020. PMID: 31977013 Free PMC article.
Impact of systolic dysfunction in genotyped hypertrophic cardiomyopathy.
Fujino N, Konno T, Hayashi K, Hodatsu A, Fujita T, Tsuda T, Nagata Y, Kawashiri MA, Ino H, Yamagishi M. Fujino N, et al. Among authors: hodatsu a. Clin Cardiol. 2013 Mar;36(3):160-5. doi: 10.1002/clc.22082. Epub 2012 Nov 29. Clin Cardiol. 2013. PMID: 23197398 Free PMC article.
21 results