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Genetic variation in angiotensin II type 2 receptor gene influences extent of left ventricular hypertrophy in hypertrophic cardiomyopathy independent of blood pressure.
Carstens N, van der Merwe L, Revera M, Heradien M, Goosen A, Brink PA, Moolman-Smook JC. Carstens N, et al. Among authors: brink pa. J Renin Angiotensin Aldosterone Syst. 2011 Sep;12(3):274-80. doi: 10.1177/1470320310390725. Epub 2010 Dec 16. J Renin Angiotensin Aldosterone Syst. 2011. PMID: 21163866 Free article.
Abnormal blood pressure response to exercise occurs more frequently in hypertrophic cardiomyopathy patients with the R92W troponin T mutation than in those with myosin mutations.
Heradien M, Revera M, van der Merwe L, Goosen A, Corfield VA, Brink PA, Mayosi BM, Moolman-Smook JC. Heradien M, et al. Among authors: brink pa. Heart Rhythm. 2009 Nov;6(11 Suppl):S18-24. doi: 10.1016/j.hrthm.2009.07.020. Epub 2009 Sep 1. Heart Rhythm. 2009. PMID: 19880069 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: brink pa. 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.
89 results