These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
347 related articles for article (PubMed ID: 28749435)
1. Allelic Complexity in Long QT Syndrome: A Family-Case Study. Zullo A; Frisso G; Detta N; Sarubbi B; Romeo E; Cordella A; Vanoye CG; Calabrò R; George AL; Salvatore F Int J Mol Sci; 2017 Jul; 18(8):. PubMed ID: 28749435 [TBL] [Abstract][Full Text] [Related]
2. Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2. Cordeiro JM; Perez GJ; Schmitt N; Pfeiffer R; Nesterenko VV; Burashnikov E; Veltmann C; Borggrefe M; Wolpert C; Schimpf R; Antzelevitch C Can J Physiol Pharmacol; 2010 Dec; 88(12):1181-90. PubMed ID: 21164565 [TBL] [Abstract][Full Text] [Related]
3. Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations. Zhang X; Chen S; Zhang L; Liu M; Redfearn S; Bryant RM; Oberti C; Vincent GM; Wang QK BMC Med Genet; 2008 Sep; 9():87. PubMed ID: 18808722 [TBL] [Abstract][Full Text] [Related]
4. Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: evidence for clinically significant IKr-IKs alpha-subunit interaction. Biliczki P; Girmatsion Z; Brandes RP; Harenkamp S; Pitard B; Charpentier F; Hébert TE; Hohnloser SH; Baró I; Nattel S; Ehrlich JR Heart Rhythm; 2009 Dec; 6(12):1792-801. PubMed ID: 19959132 [TBL] [Abstract][Full Text] [Related]
5. Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome. Grunnet M; Behr ER; Calloe K; Hofman-Bang J; Till J; Christiansen M; McKenna WJ; Olesen SP; Schmitt N Heart Rhythm; 2005 Nov; 2(11):1238-49. PubMed ID: 16253915 [TBL] [Abstract][Full Text] [Related]
6. 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]
8. [Novel mutations of potassium channel KCNQ1 S145L and KCNH2 Y475C genes in Chinese pedigrees of long QT syndrome]. Liu WL; Hu DY; Li P; Li CL; Qin XG; Li YT; Li L; Li ZM; Dong W; Qi Y; Wang Q Zhonghua Nei Ke Za Zhi; 2006 Jun; 45(6):463-6. PubMed ID: 16831322 [TBL] [Abstract][Full Text] [Related]
9. Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance. Barc J; Briec F; Schmitt S; Kyndt F; Le Cunff M; Baron E; Vieyres C; Sacher F; Redon R; Le Caignec C; Le Marec H; Probst V; Schott JJ J Am Coll Cardiol; 2011 Jan; 57(1):40-7. PubMed ID: 21185499 [TBL] [Abstract][Full Text] [Related]
10. Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients. Chang YS; Yang YW; Lin YN; Lin KH; Chang KC; Chang JG Int Heart J; 2015; 56(4):450-3. PubMed ID: 26118593 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome. Liu L; Hayashi K; Kaneda T; Ino H; Fujino N; Uchiyama K; Konno T; Tsuda T; Kawashiri MA; Ueda K; Higashikata T; Shuai W; Kupershmidt S; Higashida H; Yamagishi M Heart Rhythm; 2013 Jan; 10(1):61-7. PubMed ID: 23010577 [TBL] [Abstract][Full Text] [Related]
13. A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndrome. Aizawa Y; Ueda K; Scornik F; Cordeiro JM; Wu Y; Desai M; Guerchicoff A; Nagata Y; Iesaka Y; Kimura A; Hiraoka M; Antzelevitch C J Cardiovasc Electrophysiol; 2007 Sep; 18(9):972-7. PubMed ID: 17655673 [TBL] [Abstract][Full Text] [Related]
14. Investigation of ion channel gene variants in patients with long QT syndrome. Ernesto C; Cruz FE; Lima FS; Coutinho JL; Silva R; Urményi TP; Carvalho AC; Rondinelli E Arq Bras Cardiol; 2011 Mar; 96(3):172-8. PubMed ID: 21308345 [TBL] [Abstract][Full Text] [Related]
15. Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome. Eddy CA; MacCormick JM; Chung SK; Crawford JR; Love DR; Rees MI; Skinner JR; Shelling AN Heart Rhythm; 2008 Sep; 5(9):1275-81. PubMed ID: 18774102 [TBL] [Abstract][Full Text] [Related]
16. A hERG mutation E1039X produced a synergistic lesion on I Wu J; Mizusawa Y; Ohno S; Ding WG; Higaki T; Wang Q; Kohjitani H; Makiyama T; Itoh H; Toyoda F; James AF; Hancox JC; Matsuura H; Horie M Sci Rep; 2018 Feb; 8(1):3129. PubMed ID: 29449639 [TBL] [Abstract][Full Text] [Related]
17. KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome. Crotti L; Lundquist AL; Insolia R; Pedrazzini M; Ferrandi C; De Ferrari GM; Vicentini A; Yang P; Roden DM; George AL; Schwartz PJ Circulation; 2005 Aug; 112(9):1251-8. PubMed ID: 16116052 [TBL] [Abstract][Full Text] [Related]
18. Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications. Shinwari ZM; Al-Hazzani A; Dzimiri N; Tulbah S; Mallawi Y; Al-Fayyadh M; Al-Hassnan ZN Clin Genet; 2013 Apr; 83(4):370-4. PubMed ID: 22708720 [TBL] [Abstract][Full Text] [Related]