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Mutations in Kir2. 1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome NM Plaster, R Tawil, M Tristani-Firouzi, S Canún, S Bendahhou, ... Cell 105 (4), 511-519, 2001 | 1202 | 2001 |
Molecular mechanism for an inherited cardiac arrhythmia PB Bennett, K Yazawa, N Makita, AL George Jr Nature 376 (6542), 683-685, 1995 | 1160 | 1995 |
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Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A) DW Benson, DW Wang, M Dyment, TK Knilans, FA Fish, MJ Strieper, ... The Journal of clinical investigation 112 (7), 1019-1028, 2003 | 726 | 2003 |
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A common polymorphism associated with antibiotic-induced cardiac arrhythmia F Sesti, GW Abbott, J Wei, KT Murray, S Saksena, PJ Schwartz, SG Priori, ... Proceedings of the National Academy of Sciences 97 (19), 10613-10618, 2000 | 641 | 2000 |
PiggyBac transposon-mediated gene transfer in human cells MH Wilson, CJ Coates, AL George Molecular therapy 15 (1), 139-145, 2007 | 598 | 2007 |
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Inherited disorders of voltage-gated sodium channels AL George The Journal of clinical investigation 115 (8), 1990-1999, 2005 | 486 | 2005 |
Identification of a mutation in the gene causing hyperkalemic periodic paralysis LJ Ptáček, AL George Jr, RC Griggs, R Tawil, RG Kallen, RL Barchi, ... Cell 67 (5), 1021-1027, 1991 | 471 | 1991 |
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Molecular basis of an inherited epilepsy C Lossin, DW Wang, TH Rhodes, CG Vanoye, AL George Neuron 34 (6), 877-884, 2002 | 441 | 2002 |
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