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The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote.
Hedley PL, Kanters JK, Dembic M, Jespersen T, Skibsbye L, Aidt FH, Eschen O, Graff C, Behr ER, Schlamowitz S, Corfield V, McKenna WJ, Christiansen M. Hedley PL, et al. Among authors: corfield v. Circ Cardiovasc Genet. 2013 Oct;6(5):452-61. doi: 10.1161/CIRCGENETICS.113.000137. Epub 2013 Sep 10. Circ Cardiovasc Genet. 2013. PMID: 24021552
The genetic basis of long QT and short QT syndromes: a mutation update.
Hedley PL, Jørgensen P, Schlamowitz S, Wangari R, Moolman-Smook J, Brink PA, Kanters JK, Corfield VA, Christiansen M. Hedley PL, et al. Among authors: corfield va. Hum Mutat. 2009 Nov;30(11):1486-511. doi: 10.1002/humu.21106. Hum Mutat. 2009. PMID: 19862833 Review.
The genetic basis of Brugada syndrome: a mutation update.
Hedley PL, Jørgensen P, Schlamowitz S, Moolman-Smook J, Kanters JK, Corfield VA, Christiansen M. Hedley PL, et al. Among authors: corfield va. Hum Mutat. 2009 Sep;30(9):1256-66. doi: 10.1002/humu.21066. Hum Mutat. 2009. PMID: 19606473 Review.
Long QT syndrome in South Africa: the results of comprehensive genetic screening.
Hedley PL, Durrheim GA, Hendricks F, Goosen A, Jespersgaard C, Støvring B, Pham TT, Christiansen M, Brink PA, Corfield VA. Hedley PL, et al. Among authors: corfield va. Cardiovasc J Afr. 2013 Jul;24(6):231-7. doi: 10.5830/CVJA-2013-032. Cardiovasc J Afr. 2013. PMID: 24217263 Free PMC article.
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1.
de Villiers CP, van der Merwe L, Crotti L, Goosen A, George AL Jr, Schwartz PJ, Brink PA, Moolman-Smook JC, Corfield VA. de Villiers CP, et al. Among authors: corfield va. Circ Cardiovasc Genet. 2014 Oct;7(5):599-606. doi: 10.1161/CIRCGENETICS.113.000580. Epub 2014 Aug 2. Circ Cardiovasc Genet. 2014. PMID: 25087618 Free PMC article.
Filamin C: a novel component of the KCNE2 interactome during hypoxia.
Neethling A, Mouton J, Loos B, Corfield V, de Villiers C, Kinnear C. Neethling A, et al. Among authors: corfield v. Cardiovasc J Afr. 2016 Jan-Feb;27(1):4-11. doi: 10.5830/CVJA-2015-049. Cardiovasc J Afr. 2016. PMID: 26956495 Free PMC article.
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.
Schwartz PJ, Priori SG, Spazzolini C, Moss AJ, Vincent GM, Napolitano C, Denjoy I, Guicheney P, Breithardt G, Keating MT, Towbin JA, Beggs AH, Brink P, Wilde AA, Toivonen L, Zareba W, Robinson JL, Timothy KW, Corfield V, Wattanasirichaigoon D, Corbett C, Haverkamp W, Schulze-Bahr E, Lehmann MH, Schwartz K, Coumel P, Bloise R. Schwartz PJ, et al. Among authors: corfield v. Circulation. 2001 Jan 2;103(1):89-95. doi: 10.1161/01.cir.103.1.89. Circulation. 2001. PMID: 11136691 Clinical Trial.
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.
Andersen PS, Havndrup O, Bundgaard H, Moolman-Smook JC, Larsen LA, Mogensen J, Brink PA, Børglum AD, Corfield VA, Kjeldsen K, Vuust J, Christiansen M. Andersen PS, et al. Among authors: corfield va. J Med Genet. 2001 Dec;38(12):E43. doi: 10.1136/jmg.38.12.e43. J Med Genet. 2001. PMID: 11748309 Free PMC article. No abstract available.
56 results