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Sudden infant death syndrome and inherited cardiac conditions.
Baruteau AE, Tester DJ, Kapplinger JD, Ackerman MJ, Behr ER. Baruteau AE, et al. Among authors: behr er. Nat Rev Cardiol. 2017 Dec;14(12):715-726. doi: 10.1038/nrcardio.2017.129. Epub 2017 Sep 7. Nat Rev Cardiol. 2017. PMID: 28880023 Review.
A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation.
Bartos DC, Anderson JB, Bastiaenen R, Johnson JN, Gollob MH, Tester DJ, Burgess DE, Homfray T, Behr ER, Ackerman MJ, Guicheney P, Delisle BP. Bartos DC, et al. Among authors: behr er. J Cardiovasc Electrophysiol. 2013 May;24(5):562-9. doi: 10.1111/jce.12068. Epub 2013 Jan 25. J Cardiovasc Electrophysiol. 2013. PMID: 23350853 Free PMC article.
Brugada syndrome: an update.
Li A, Behr ER. Li A, et al. Among authors: behr er. Future Cardiol. 2013 Mar;9(2):253-71. doi: 10.2217/fca.12.82. Future Cardiol. 2013. PMID: 23463977 Review.
278 results