PubMed (OMIM) for id: 10008

Year	Number of Results
1999	1
2000	1
2001	1
2002	1
2003	1
2004	3
2005	1
2006	1
2007	1
2008	1
2009	1
2012	1
2024	0

1

KCNE3 T4A as the genetic basis of Brugada-pattern electrocardiogram.

Nakajima T, Wu J, Kaneko Y, Ashihara T, Ohno S, Irie T, Ding WG, Matsuura H, Kurabayashi M, Horie M. Nakajima T, et al. Circ J. 2012;76(12):2763-72. doi: 10.1253/circj.cj-12-0551. Epub 2012 Sep 13. Circ J. 2012. PMID: 22987075 Free article.

2

Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.

Ohno S, Toyoda F, Zankov DP, Yoshida H, Makiyama T, Tsuji K, Honda T, Obayashi K, Ueyama H, Shimizu W, Miyamoto Y, Kamakura S, Matsuura H, Kita T, Horie M. Ohno S, et al. Hum Mutat. 2009 Apr;30(4):557-63. doi: 10.1002/humu.20834. Hum Mutat. 2009. PMID: 19306396

3

Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome.

Delpón E, Cordeiro JM, Núñez L, Thomsen PE, Guerchicoff A, Pollevick GD, Wu Y, Kanters JK, Larsen CT, Hofman-Bang J, Burashnikov E, Christiansen M, Antzelevitch C. Delpón E, et al. Circ Arrhythm Electrophysiol. 2008 Aug;1(3):209-18. doi: 10.1161/CIRCEP.107.748103. Circ Arrhythm Electrophysiol. 2008. PMID: 19122847 Free PMC article.

4

Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis.

Jurkat-Rott K, Lehmann-Horn F. Jurkat-Rott K, et al. Neurotherapeutics. 2007 Apr;4(2):216-24. doi: 10.1016/j.nurt.2007.02.001. Neurotherapeutics. 2007. PMID: 17395131 Free article. Review.

5

Phosphorylation and protonation of neighboring MiRP2 sites: function and pathophysiology of MiRP2-Kv3.4 potassium channels in periodic paralysis.

Abbott GW, Butler MH, Goldstein SA. Abbott GW, et al. FASEB J. 2006 Feb;20(2):293-301. doi: 10.1096/fj.05-5070com. FASEB J. 2006. PMID: 16449802 Free article.

6

Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

Antzelevitch C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, Gussak I, LeMarec H, Nademanee K, Perez Riera AR, Shimizu W, Schulze-Bahr E, Tan H, Wilde A. Antzelevitch C, et al. Circulation. 2005 Feb 8;111(5):659-70. doi: 10.1161/01.CIR.0000152479.54298.51. Epub 2005 Jan 17. Circulation. 2005. PMID: 15655131 Review.

7

No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients.

Tang NL, Chow CC, Ko GT, Tai MH, Kwok R, Yao XQ, Cockram CS. Tang NL, et al. Clin Endocrinol (Oxf). 2004 Jul;61(1):109-12. doi: 10.1111/j.1365-2265.2004.02079.x. Clin Endocrinol (Oxf). 2004. PMID: 15212652

8

KCNE1 binds to the KCNQ1 pore to regulate potassium channel activity.

Melman YF, Um SY, Krumerman A, Kagan A, McDonald TV. Melman YF, et al. Neuron. 2004 Jun 24;42(6):927-37. doi: 10.1016/j.neuron.2004.06.001. Neuron. 2004. PMID: 15207237 Free article.

9

Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation.

Jurkat-Rott K, Lehmann-Horn F. Jurkat-Rott K, et al. Neurology. 2004 Mar 23;62(6):1012-5. doi: 10.1212/01.wnl.0000119392.29624.88. Neurology. 2004. PMID: 15037716

10

Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis.

Sternberg D, Tabti N, Fournier E, Hainque B, Fontaine B. Sternberg D, et al. Neurology. 2003 Sep 23;61(6):857-9. doi: 10.1212/01.wnl.0000082392.66713.e3. Neurology. 2003. PMID: 14504341

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