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5. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population. Liu W; Yang J; Hu D; Kang C; Li C; Zhang S; Li P; Chen Z; Qin X; Ying K; Li Y; Li Y; Li Z; Cheng X; Li L; Qi Y; Chen S; Wang Q Hum Mutat; 2002 Dec; 20(6):475-6. PubMed ID: 12442276 [TBL] [Abstract][Full Text] [Related]
6. Short QT syndrome. What is it? Where is it? Puri VK; Dwivedi SK; Puri A; Behal K Indian Heart J; 2005; 57(6):769-71. PubMed ID: 16521657 [No Abstract] [Full Text] [Related]
7. Compound heterozygosity for mutations Asp611-->Tyr in KCNQ1 and Asp609-->Gly in KCNH2 associated with severe long QT syndrome. Yamaguchi M; Shimizu M; Ino H; Terai H; Hayashi K; Kaneda T; Mabuchi H; Sumita R; Oshima T; Hoshi N; Higashida H Clin Sci (Lond); 2005 Feb; 108(2):143-50. PubMed ID: 15500450 [TBL] [Abstract][Full Text] [Related]
8. A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels. Hasegawa K; Ohno S; Ashihara T; Itoh H; Ding WG; Toyoda F; Makiyama T; Aoki H; Nakamura Y; Delisle BP; Matsuura H; Horie M Heart Rhythm; 2014 Jan; 11(1):67-75. PubMed ID: 24096004 [TBL] [Abstract][Full Text] [Related]
9. Short QT syndrome: a case report and review of literature. Lu LX; Zhou W; Zhang X; Cao Q; Yu K; Zhu C Resuscitation; 2006 Oct; 71(1):115-21. PubMed ID: 16942825 [TBL] [Abstract][Full Text] [Related]
10. Short QT syndrome: a very rare arrhythmogenic entity. Yontar OC; Yalta K; Yilmaz MB; Turgut OO Acta Cardiol; 2008 Oct; 63(5):553-5. PubMed ID: 19013996 [TBL] [Abstract][Full Text] [Related]
12. Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing. Muñoz-Esparza C; García-Molina E; Salar-Alcaraz M; Peñafiel-Verdú P; Sánchez-Muñoz JJ; Martínez Sánchez J; Cabañas-Perianes V; Valdés Chávarri M; García Alberola A; Gimeno-Blanes JR Rev Esp Cardiol (Engl Ed); 2015 Oct; 68(10):861-8. PubMed ID: 25819988 [TBL] [Abstract][Full Text] [Related]
13. Genetic variants of potassium voltage-gated channel genes (KCNQ1, KCNH2, and KCNE1) affected the risk of atrial fibrillation in elderly patients. Li L; Shen C; Yao Z; Liang J; Huang C Genet Test Mol Biomarkers; 2015 Jul; 19(7):359-65. PubMed ID: 26066992 [TBL] [Abstract][Full Text] [Related]
14. [A novel KCNQ1 mutation in Chinese with congenital long QT syndrome]. Liang L; Du ZD; Cai LL; Wu JX; Zheng T; Qi TX Zhonghua Er Ke Za Zhi; 2003 Oct; 41(10):724-7. PubMed ID: 14731347 [TBL] [Abstract][Full Text] [Related]
15. Modulation of I(Kr) inactivation by mutation N588K in KCNH2: a link to arrhythmogenesis in short QT syndrome. Cordeiro JM; Brugada R; Wu YS; Hong K; Dumaine R Cardiovasc Res; 2005 Aug; 67(3):498-509. PubMed ID: 16039272 [TBL] [Abstract][Full Text] [Related]
16. Genetic modifier of the QTc interval associated with early-onset atrial fibrillation. Andreasen L; Nielsen JB; Christophersen IE; Holst AG; Sajadieh A; Tveit A; Haunsø S; Svendsen JH; Schmitt N; Olesen MS Can J Cardiol; 2013 Oct; 29(10):1234-40. PubMed ID: 24074973 [TBL] [Abstract][Full Text] [Related]
17. Clinical characteristics and treatment of short QT syndrome. Wolpert C; Schimpf R; Veltmann C; Giustetto C; Gaita F; Borggrefe M Expert Rev Cardiovasc Ther; 2005 Jul; 3(4):611-7. PubMed ID: 16076272 [TBL] [Abstract][Full Text] [Related]