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Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|July 2, 2008
Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathyMaximilian G Posch, Laura Thiemann, Pavol Tomasov, et al.International Journal of Cardiology|May 29, 2013
Variations in the human soluble epoxide hydrolase gene and recurrence of atrial fibrillation after catheter ablationAlexander Wutzler, Christoph Kestler, Andreas Perrot, et al.Pediatric Cardiology|August 20, 2014
CCN1 mutation is associated with atrial septal defectAndreas Perrot, Katharina R Schmitt, Eva-Maria G Roth, et al.Disease Markers|December 20, 2008
Mitochondrial transcription factors TFA, TFB1 and TFB2: a search for DNA variants/haplotypes and the risk of cardiac hypertrophyCristina Alonso-Montes, Mónica G Castro, Julián R Reguero, et al.Human Molecular Genetics|January 25, 2014
Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of FallotMarcel Grunert, Cornelia Dorn, Markus Schueler, et al.Basic Research in Cardiology|July 20, 2011
Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathySnigdha Tripathi, Imke Schultz, Edgar Becker, et al.European Journal of Heart Failure|January 3, 2006
Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriersAndreas Perrot, Holger H Sigusch, Herbert Nägele, et al.Journal of Molecular and Cellular Cardiology|October 5, 2023
Nonsense mediated decay factor UPF3B is associated with cMyBP-C haploinsufficiency in hypertrophic cardiomyopathy patientsValentin Burkart, Kathrin Kowalski, Alina Disch, et al.Molecular Genetics and Metabolism|August 6, 2008
A missense variant in desmoglein-2 predisposes to dilated cardiomyopathyMaximilian G Posch, Matthias J Posch, Christian Geier, et al.Human Mutation|April 15, 2008
A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathySiv Fokstuen, Robert Lyle, Analia Munoz, et al.Pageof 7