Search Results - "DAO, Dmi"

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia by MCNAIR, William P, KU, Lisa, TAYLOR, Matthew R. G, FAIN, Pam R, DAO, Dmi, WOLFEL, Eugene, MESTRONI, Luisa

“…We studied a large family affected by an autosomal dominant cardiac conduction disorder associated with sinus node dysfunction, arrhythmia, and right and…”
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α-myosin heavy chain : A sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy by CARNIEL, Elisa, TAYLOR, Matthew R. G, GRAW, Sharon L, FEIGER, Jennie, XIAO ZHONG ZHU, DAO, Dmi, FERGUSON, Debra A, BRISTOW, Michael R, MESTRONI, Luisa, SINAGRA, Gianfranco, DI LENARDA, Andrea, KU, Lisa, FAIN, Pamela R, BOUCEK, Mark M, CAVANAUGH, Mi Jean, MIOCIC, Snjezana, SLAVOV, Dobromir

“…Mutations in the beta-myosin heavy-chain (betaMyHC) gene cause hypertrophic (HCM) and dilated (DCM) forms of cardiomyopathy. In failing human hearts,…”
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Natural history of dilated cardiomyopathy due to lamin A/C gene mutations by Taylor, Matthew R.G, Fain, Pamela R, Sinagra, Gianfranco, Robinson, Misi L, Robertson, Alastair D, Carniel, Elisa, Di Lenarda, Andrea, Bohlmeyer, Teresa J, Ferguson, Debra A, Brodsky, Gary L, Boucek, Mark M, Lascor, Jean, Moss, Andrew C, Li, Wai-Lun P, Stetler, Gary L, Muntoni, Francesco, Bristow, Michael R, Mestroni, Luisa

“…We examined the prevalence, genotype-phenotype correlation, and natural history of lamin A/C gene (LMNA) mutations in subjects with dilated cardiomyopathy…”
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