Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Reference30 articles.
1. Thiene G, Corrado D, Basso C: Arrhythmogenic right ventricular cardiomyopathy/dysplasia. Orphanet J Rare Dis 2007, 2: 45–61.
2. Eckhardt LL, Farley AL, Rodriguez E, et al.: KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties. Heart Rhythm 2007, 4: 323–329.
3. Tan HL, Bardai A, Shimizu W, et al.: Genotype-specific onset of arrhythmia in congenital long-QT syndrome: possible therapy implications. Circulation 2006, 114: 1096–1103.
4. Hayashi M, Takatsuki S, Maison-Blanche P, et al.: Ventricular repolarization restitution properties in patients exhibiting type 1 Brugada electrocardiogram with and without inducible ventricular fibrillation. J Am Coll Cardiol 2008, 51: 1162–1168.
5. London B, Michalec M, Mehdi H, et al.: Mutation in glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias. Circulation 2007, 116: 2260–2268.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献