Author:
Neyroud Nathalie,Tesson Frédérique,Denjoy Isabelle,Leibovici Michel,Donger Claire,Barhanin Jacques,Fauré Sabine,Gary Françoise,Coumel Philippe,Petit Christine,Schwartz Ketty,Guicheney Pascale
Publisher
Springer Science and Business Media LLC
Reference31 articles.
1. Jervell, A. & Lange-Nielsen, F. Congenital deaf mutism, functional heart disease with prolongation of the QT interval and sudden death. Am. Heart J. 54, 59–68 (1956).
2. Fraser, G.R., Froggatt, P. & Murphy, T. Genetical aspects of the cardio-auditory syndrome of Jervell and Lange-Nielsen (congenital deafness and electrocardiographic abnormalities). Ann. Hum. Genet. 28, 133–157 (1964).
3. Pernot, C., Henry, M. & Debruille, C. Les syndromes cardio-auditifs d'origine génétique.. Coeur Méd Interne 13, 429–443 (1974).
4. Schwartz, P.J., Periti, M. & Malliani, A. The long Q-T syndrome. Am. Heart J. 89, 378–390 (1975).
5. Wang, Q. et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nature Genet 12, 17–23 (1996).
Cited by
776 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