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Journal of Cardiovascular Electrophysiology|February 13, 2008
X-linked nonsyndromic sinus node dysfunction and atrial fibrillation caused by emerin mutationMargaret L Karst, Kathleen J Herron, Timothy M OlsonCirculation|May 22, 2002
Myosin light chain mutation causes autosomal recessive cardiomyopathy with mid-cavitary hypertrophy and restrictive physiologyTimothy M Olson, Margaret L Karst, Frank G Whitby, et al.Journal of the American College of Cardiology|August 29, 2009
Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathyKatharine M Brauch, Margaret L Karst, Kathleen J Herron, et al.JAMA|January 27, 2005
Sodium channel mutations and susceptibility to heart failure and atrial fibrillationTimothy M Olson, Virginia V Michels, Jeffrey D Ballew, et al.The New England Journal of Medicine|July 11, 2008
Atrial natriuretic peptide frameshift mutation in familial atrial fibrillationDenice M Hodgson-Zingman, Margaret L Karst, Leonid V Zingman, et al.Pageof 1