Founder mutations in inherited cardiac diseases in the by Arthur A.M. Wilde, J. Peter van Tintelen

By Arthur A.M. Wilde, J. Peter van Tintelen

This e-book summarizes our present wisdom of founder mutation populations (‘extended families’) within the Netherlands, between different elements delivering perception in the place those sufferers may be anticipated (coloured maps of the superiority within the ninety nine Dutch postal code areas are supplied for each phenotype) and what their designated phenotype is.

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Maron BJ, Casey SA, Poliac LC, Gohman TE, Almquist AK, Aeppli DM. Clinical course of hypertrophic cardiomyopathy in a regional United States cohort. JAMA. 1999;281:650-5. Kofflard MJ, Waldstein DJ, Vos J, Ten Cate FJ. Prognosis in hypertrophic cardiomyopathy observed in a large clinic population. Am J Cardiol. 1993;72:939-43.

2009;17:422–8. 10. van den Berg MP, Wilde AA, Viersma JW, et al. Possible bradycardic mode of death and successful pacemaker treatment in a large family with features of long QT syndrome type 3 and Brugada syndrome. J Cardiovasc Electrophysiol. 2001;12:630–6. 11. Sijbrands EJ, Westendorp RG, Defesche JC, et al. Mortality over two centuries in large pedigree with familial hypercholesterolaemia: family tree mortality study. BMJ. 2001;322:1019–23. 35 References 12. Tung R, Zimetbaum P, Josephson ME.

Postema PG, Wolpert C, Amin AS, Probst V, Borggrefe M, Roden DM, et al. org). Heart Rhythm. 2009;6:1335–41. 37. Scicluna BP, Wilde AW, Bezzina CR. The primary arrhythmia syndromes: same mutation, different manifestations. Are we starting to understand why? J Cardiovasc Electrophysiol. 2008;19:445–52. G. Postema, I. Christiaans, N. Hofman, M. T. R. Bezzina, P. Loh, K. A. M. Wilde Abstract In this part of a series on founder mutations in the Netherlands, we review familial idiopathic ventricular fibrillation linked to the DPP6 gene.

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