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Journal of Cardiovascular Electrophysiology|March 28, 2008
Lone atrial fibrillation: influence of familial disease on gender predilectionLin Y Chen, Kathleen J Herron, Bee C Tai, et al.Circulation|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 Heart Association|December 15, 2015
Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated CardiomyopathyPamela A Long, Brandon T Larsen, Jared M Evans, et al.Human Genetics|August 18, 2009
KATP channel Kir6.2 E23K variant overrepresented in human heart failure is associated with impaired exercise stress responseSantiago Reyes, Sungjo Park, Bruce D Johnson, et al.European Journal of Heart Failure|August 19, 2014
Characterizing genetic variation of adrenergic signalling pathways in Takotsubo (stress) cardiomyopathy exomesAdele H Goodloe, Jared M Evans, Sumit Middha, et al.Journal of Molecular and Cellular Cardiology|May 25, 2005
Cardiac KATP channels in health and diseaseGarvan C Kane, Xiao-Ke Liu, Satsuki Yamada, et al.American Journal of Medical Genetics. Part A|May 14, 2016
Ebstein anomaly, left ventricular non-compaction, and early onset heart failure associated with a de novo α-tropomyosin gene mutationAngela M Kelle, S Jared Bentley, Luis O Rohena, et al.JAMA Internal Medicine|March 24, 2015
Familial spontaneous coronary artery dissection: evidence for genetic susceptibilityKashish Goel, Marysia Tweet, Timothy M Olson, et al.The American Journal of Cardiology|October 5, 2015
Familial Incidence of Cardiovascular Malformations in Hypoplastic Left Heart SyndromeAngela M Kelle, Muhammad Y Qureshi, Timothy M Olson, et al.Pediatrics in Review|July 3, 2019
Hypoplastic Left Heart Syndrome: An Overview for Primary Care ProvidersRabia Javed, Frank Cetta, Sameh M Said, et al.Pageof 8