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Increased burden of cardiovascular disease in carriers of APOL1 genetic variants.
Ito K, Bick AG, Flannick J, Friedman DJ, Genovese G, Parfenov MG, Depalma SR, Gupta N, Gabriel SB, Taylor HA Jr, Fox ER, Newton-Cheh C, Kathiresan S, Hirschhorn JN, Altshuler DM, Pollak MR, Wilson JG, Seidman JG, Seidman C. Ito K, et al. Among authors: seidman jg, seidman c. Circ Res. 2014 Feb 28;114(5):845-50. doi: 10.1161/CIRCRESAHA.114.302347. Epub 2013 Dec 30. Circ Res. 2014. PMID: 24379297 Free PMC article.
Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
Watkins H, Thierfelder L, Hwang DS, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. J Clin Invest. 1992 Nov;90(5):1666-71. doi: 10.1172/JCI116038. J Clin Invest. 1992. PMID: 1430197 Free PMC article.
Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
Solomon SD, Jarcho JA, McKenna W, Geisterfer-Lowrance A, Germain R, Salerni R, Seidman JG, Seidman CE. Solomon SD, et al. Among authors: seidman jg, seidman ce. J Clin Invest. 1990 Sep;86(3):993-9. doi: 10.1172/JCI114802. J Clin Invest. 1990. PMID: 1975599 Free PMC article.
592 results