Similar articles for PMID: 23010577

Year	Number of Results
1996	1
1998	2
1999	3
2000	2
2002	4
2003	2
2004	3
2005	10
2006	16
2007	12
2008	17
2009	15
2010	15
2011	14
2012	19
2013	23
2014	10
2015	15
2016	15
2017	11
2018	16
2019	15
2020	13
2021	17
2022	15
2023	5
2024	0

1

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. Liu L, et al. Heart Rhythm. 2013 Jan;10(1):61-7. doi: 10.1016/j.hrthm.2012.09.053. Epub 2012 Sep 23. Heart Rhythm. 2013. PMID: 23010577

2

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. Liu W, et al. Hum Mutat. 2002 Dec;20(6):475-6. doi: 10.1002/humu.9085. Hum Mutat. 2002. PMID: 12442276 Free PMC article.

3

[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. Liu WL, et al. Zhonghua Nei Ke Za Zhi. 2006 Jun;45(6):463-6. Zhonghua Nei Ke Za Zhi. 2006. PMID: 16831322 Chinese.

4

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. Barc J, et al. J Am Coll Cardiol. 2011 Jan 4;57(1):40-7. doi: 10.1016/j.jacc.2010.08.621. J Am Coll Cardiol. 2011. PMID: 21185499 Free article.

5

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. Yamaguchi M, et al. Clin Sci (Lond). 2005 Feb;108(2):143-50. doi: 10.1042/CS20040220. Clin Sci (Lond). 2005. PMID: 15500450

6

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. Biliczki P, et al. Heart Rhythm. 2009 Dec;6(12):1792-801. doi: 10.1016/j.hrthm.2009.08.009. Epub 2009 Aug 13. Heart Rhythm. 2009. PMID: 19959132

7

HERG-F463L potassium channels linked to long QT syndrome reduce I(Kr) current by a trafficking-deficient mechanism.

Yang HT, Sun CF, Cui CC, Xue XL, Zhang AF, Li HB, Wang DQ, Shu J. Yang HT, et al. Clin Exp Pharmacol Physiol. 2009 Aug;36(8):822-7. doi: 10.1111/j.1440-1681.2009.05150.x. Clin Exp Pharmacol Physiol. 2009. PMID: 19215240

8

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. Grunnet M, et al. Heart Rhythm. 2005 Nov;2(11):1238-49. doi: 10.1016/j.hrthm.2005.07.025. Heart Rhythm. 2005. PMID: 16253915

9

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. Zhang X, et al. BMC Med Genet. 2008 Sep 23;9:87. doi: 10.1186/1471-2350-9-87. BMC Med Genet. 2008. PMID: 18808722 Free PMC article.

10

Clinical characteristics of 30 Czech families with long QT syndrome and KCNQ1 and KCNH2 gene mutations: importance of exercise testing.

Andrsova I, Novotny T, Kadlecova J, Bittnerova A, Vit P, Florianova A, Sisakova M, Gaillyova R, Manouskova L, Spinar J. Andrsova I, et al. J Electrocardiol. 2012 Nov-Dec;45(6):746-51. doi: 10.1016/j.jelectrocard.2012.05.004. Epub 2012 Jun 22. J Electrocardiol. 2012. PMID: 22727609

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