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Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome.
Zareba W, Moss AJ, Sheu G, Kaufman ES, Priori S, Vincent GM, Towbin JA, Benhorin J, Schwartz PJ, Napolitano C, Hall WJ, Keating MT, Qi M, Robinson J, Andrews ML; International LQTS Registry, University of Rochester, Rochester, New York. Zareba W, et al. J Cardiovasc Electrophysiol. 2003 Nov;14(11):1149-53. doi: 10.1046/j.1540-8167.2003.03177.x. J Cardiovasc Electrophysiol. 2003. PMID: 14678125
New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
Li H, Chen Q, Moss AJ, Robinson J, Goytia V, Perry JC, Vincent GM, Priori SG, Lehmann MH, Denfield SW, Duff D, Kaine S, Shimizu W, Schwartz PJ, Wang Q, Towbin JA. Li H, et al. Circulation. 1998 Apr 7;97(13):1264-9. doi: 10.1161/01.cir.97.13.1264. Circulation. 1998. PMID: 9570196
Long QT syndrome.
Moss AJ, Robinson JL. Moss AJ, et al. Among authors: robinson jl. Heart Dis Stroke. 1992 Sep-Oct;1(5):309-14. Heart Dis Stroke. 1992. PMID: 1344123 Review. No abstract available.
Clinical aspects of the idiopathic long QT syndrome.
Moss AJ, Robinson JL. Moss AJ, et al. Among authors: robinson jl. Ann N Y Acad Sci. 1992 Jan 27;644:103-11. doi: 10.1111/j.1749-6632.1992.tb31006.x. Ann N Y Acad Sci. 1992. PMID: 1348608 No abstract available.
674 results