Molecular genetics of inherited long QT syndromes

[1] Lidocaine block of LQT-3 mutant human Na+ channels [J]. CIRCULATION RESEARCH, 1996, 79 (01) : 103 - 108

[2] K(v)LQT1 and IsK (minK) proteins associate to form the I-Ks cardiac potassium current [J]. NATURE, 1996, 384 (6604) : 78 - 80

[3] Missense mutation in the pore region of HERG causes familial long QT syndrome [J]. CIRCULATION, 1996, 93 (10) : 1791 - 1795

[4] Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias [J]. EMBO JOURNAL, 1997, 16 (17) : 5472 - 5479

[5] Genetically defined therapy of inherited long-QT syndrome - Correction of abnormal repolarization by potassium [J]. CIRCULATION, 1996, 94 (05) : 1018 - 1022

[6] CURRAN C, 1993, J CLIN INVEST, V93, P799

[7] A MOLECULAR-BASIS FOR CARDIAC-ARRHYTHMIA - HERG MUTATIONS CAUSE LONG QT SYNDROME [J]. CELL, 1995, 80 (05) : 795 - 803

[8] A mutation in HERG associated with notched T waves in long QT syndrome [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1996, 28 (08) : 1609 - 1615

[9] EVIDENCE OF GENETIC AND PHENOTYPIC HETEROGENEITY IN THE ROMANO-WARD SYNDROME [J]. JOURNAL OF MEDICAL GENETICS, 1993, 30 (11) : 947 - 950

[10] Evidence of a long QT founder gene with varying phenotypic expression in South African families [J]. JOURNAL OF MEDICAL GENETICS, 1996, 33 (07) : 567 - 573

[1] Lidocaine block of LQT-3 mutant human Na+ channels [J]. CIRCULATION RESEARCH, 1996, 79 (01) : 103 - 108

[2] K(v)LQT1 and IsK (minK) proteins associate to form the I-Ks cardiac potassium current [J]. NATURE, 1996, 384 (6604) : 78 - 80

[3] Missense mutation in the pore region of HERG causes familial long QT syndrome [J]. CIRCULATION, 1996, 93 (10) : 1791 - 1795

[4] Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias [J]. EMBO JOURNAL, 1997, 16 (17) : 5472 - 5479

[5] Genetically defined therapy of inherited long-QT syndrome - Correction of abnormal repolarization by potassium [J]. CIRCULATION, 1996, 94 (05) : 1018 - 1022

[6] CURRAN C, 1993, J CLIN INVEST, V93, P799

[7] A MOLECULAR-BASIS FOR CARDIAC-ARRHYTHMIA - HERG MUTATIONS CAUSE LONG QT SYNDROME [J]. CELL, 1995, 80 (05) : 795 - 803

[8] A mutation in HERG associated with notched T waves in long QT syndrome [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1996, 28 (08) : 1609 - 1615

[9] EVIDENCE OF GENETIC AND PHENOTYPIC HETEROGENEITY IN THE ROMANO-WARD SYNDROME [J]. JOURNAL OF MEDICAL GENETICS, 1993, 30 (11) : 947 - 950

[10] Evidence of a long QT founder gene with varying phenotypic expression in South African families [J]. JOURNAL OF MEDICAL GENETICS, 1996, 33 (07) : 567 - 573