PubMed (OMIM) for id: 462303

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Year	Number of Results
1999	1
2004	2
2023	0

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Page 1

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.

Yang Y, Xia M, Jin Q, Bendahhou S, Shi J, Chen Y, Liang B, Lin J, Liu Y, Liu B, Zhou Q, Zhang D, Wang R, Ma N, Su X, Niu K, Pei Y, Xu W, Chen Z, Wan H, Cui J, Barhanin J, Chen Y. Yang Y, et al. Am J Hum Genet. 2004 Nov;75(5):899-905. doi: 10.1086/425342. Epub 2004 Sep 13. Am J Hum Genet. 2004. PMID: 15368194 Free PMC article.

KCNE2 protein is expressed in ventricles of different species, and changes in its expression contribute to electrical remodeling in diseased hearts.

Jiang M, Zhang M, Tang DG, Clemo HF, Liu J, Holwitt D, Kasirajan V, Pond AL, Wettwer E, Tseng GN. Jiang M, et al. Circulation. 2004 Apr 13;109(14):1783-8. doi: 10.1161/01.CIR.0000124225.43852.50. Epub 2004 Apr 5. Circulation. 2004. PMID: 15066947

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia.

Abbott GW, Sesti F, Splawski I, Buck ME, Lehmann MH, Timothy KW, Keating MT, Goldstein SA. Abbott GW, et al. Cell. 1999 Apr 16;97(2):175-87. doi: 10.1016/s0092-8674(00)80728-x. Cell. 1999. PMID: 10219239 Free article.

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