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Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.
Norton N, Robertson PD, Rieder MJ, Züchner S, Rampersaud E, Martin E, Li D, Nickerson DA, Hershberger RE; National Heart, Lung and Blood Institute GO Exome Sequencing Project. Norton N, et al. Among authors: hershberger re. Circ Cardiovasc Genet. 2012 Apr 1;5(2):167-74. doi: 10.1161/CIRCGENETICS.111.961805. Epub 2012 Feb 15. Circ Cardiovasc Genet. 2012. PMID: 22337857 Free PMC article.
Mutations of presenilin genes in dilated cardiomyopathy and heart failure.
Li D, Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Partain J, Nixon RR, Allen CN, Irwin RP, Jakobs PM, Litt M, Hershberger RE. Li D, et al. Among authors: hershberger re. Am J Hum Genet. 2006 Dec;79(6):1030-9. doi: 10.1086/509900. Epub 2006 Oct 24. Am J Hum Genet. 2006. PMID: 17186461 Free PMC article.
Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy.
Morales A, Painter T, Li R, Siegfried JD, Li D, Norton N, Hershberger RE. Morales A, et al. Among authors: hershberger re. Circulation. 2010 May 25;121(20):2176-82. doi: 10.1161/CIRCULATIONAHA.109.931220. Epub 2010 May 10. Circulation. 2010. PMID: 20458009 Free PMC article.
201 results