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Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome.
Cordeiro JM, Barajas-Martinez H, Hong K, Burashnikov E, Pfeiffer R, Orsino AM, Wu YS, Hu D, Brugada J, Brugada P, Antzelevitch C, Dumaine R, Brugada R. Cordeiro JM, et al. Among authors: hong k. Circulation. 2006 Nov 7;114(19):2026-33. doi: 10.1161/CIRCULATIONAHA.106.627489. Epub 2006 Oct 30. Circulation. 2006. PMID: 17075016 Free PMC article.
Sudden death associated with short-QT syndrome linked to mutations in HERG.
Brugada R, Hong K, Dumaine R, Cordeiro J, Gaita F, Borggrefe M, Menendez TM, Brugada J, Pollevick GD, Wolpert C, Burashnikov E, Matsuo K, Wu YS, Guerchicoff A, Bianchi F, Giustetto C, Schimpf R, Brugada P, Antzelevitch C. Brugada R, et al. Among authors: hong k. Circulation. 2004 Jan 6;109(1):30-5. doi: 10.1161/01.CIR.0000109482.92774.3A. Epub 2003 Dec 15. Circulation. 2004. PMID: 14676148
Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations.
Hong K, Brugada J, Oliva A, Berruezo-Sanchez A, Potenza D, Pollevick GD, Guerchicoff A, Matsuo K, Burashnikov E, Dumaine R, Towbin JA, Nesterenko V, Brugada P, Antzelevitch C, Brugada R. Hong K, et al. Circulation. 2004 Nov 9;110(19):3023-7. doi: 10.1161/01.CIR.0000144299.17008.07. Epub 2004 Nov 1. Circulation. 2004. PMID: 15520322 Free PMC article.
Brugada syndrome: 12 years of progression.
Hong K, Antzelevitch C, Brugada P, Brugada J, Ohe T, Brugada R. Hong K, et al. Acta Med Okayama. 2004 Dec;58(6):255-61. doi: 10.18926/AMO/32094. Acta Med Okayama. 2004. PMID: 15762293 Free article. Review.
Cryptic 5' splice site activation in SCN5A associated with Brugada syndrome.
Hong K, Guerchicoff A, Pollevick GD, Oliva A, Dumaine R, de Zutter M, Burashnikov E, Wu YS, Brugada J, Brugada P, Brugada R. Hong K, et al. J Mol Cell Cardiol. 2005 Apr;38(4):555-60. doi: 10.1016/j.yjmcc.2004.10.015. Epub 2004 Dec 9. J Mol Cell Cardiol. 2005. PMID: 15808832
4,790 results