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Comment
. 2019 Apr 2;139(14):1758-1759.
doi: 10.1161/CIRCULATIONAHA.118.036889.

Letter by London Regarding Article, "Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome"

Barry London  1
Affiliations
Comment

Letter by London Regarding Article, "Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome"

Barry London. Circulation. .
No abstract available

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Conflict of interest statement

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References

    1. Weiss R, Barmada MM, Nguyen T, Seibel JS, Cavlovich D, Kornblit CA, Angelilli A, Villanueva F, McNamara DM, London B. Clinical and molecular heterogeneity in the Brugada syndrome: A novel gene locus on chromosome 3. Circulation 2002;105:707–713.. - PubMed
    1. London B, Michalec M, Mehdi H, Zhu X, Kerchner L, Sanyal S, Viswanathan PC, Pfahn AE, Shang LL, Madhusudanan M, Baty CJ, Lagana S, Aleong R, Gutmann R, Ackerman MJ McNamara DM, Weis R, and Dudley SC Jr. A mutation in GPD1-L decreases cardiac Na+ current and causes inherited arrhythmias. Circulation 2007;116:2260–2268. - PMC - PubMed
    1. Van Norstrand DW, Valdivia CR, Tester DJ, Ueda K, London B, Makielski C, Ackerman MJ. Molecular and functional characterization of novel GPD1-L mutations in sudden infant death syndrome. Circulation 2007;116:2253–2259. - PMC - PubMed
    1. Hosseini SM, Kim R, Udupa S, Costain G, Jobling R, Liston E, Jamal SM, Szybowska M, Morel CF, Bowdin S, Garcia J, Care M, Sturm AC, Novelli V, Ackerman MJ, Ware JS, Hershberger RE, Wilde AAM, Gollob MH; NIH-Clinical Genome Resource Consortium. Reappraisal of Reported Genes for Sudden Arrhythmic Death: An Evidence-Based Evaluation of Gene Validity for Brugada Syndrome. Circulation. 2018;138:1195–1205. - PMC - PubMed
    1. Matasic DS, Brenner C, London B. Emerging potential benefits of modulating NAD+ metabolism in cardiovascular disease. Am J Physiol Heart Circ Physiol. 2018;314:H839–H852. - PMC - PubMed