A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions. by Gehmlich, K, Lambiase, P, Asimaki, A, Ciaccio, E, Ehler, E, Syrris, P, Saffitz, J, McKenna, W

Desmoglein-2 interaction is crucial for cardiomyocyte cohesion and function. by Schlipp, A, Schinner, C, Spindler, V, Vielmuth, F, Gehmlich, K, Syrris, P, Mckenna, W, Dendorfer, A, Hartlieb, E, Waschke, J

Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null allele. by Gehmlich, K, Syrris, P, Reimann, M, Asimaki, A, Ehler, E, Evans, A, Quarta, G, Pantazis, A, Saffitz, J, McKenna, W

Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy? by Gehmlich, K, Asimaki, A, Cahill, T, Ehler, E, Syrris, P, Zachara, E, Re, F, Avella, A, Monserrat, L, Saffitz, J, McKenna, W

Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: impact of genetics and revised task force criteria. by Quarta, G, Muir, A, Pantazis, A, Syrris, P, Gehmlich, K, Garcia-Pavia, P, Ward, D, Sen-Chowdhry, S, Elliott, P, McKenna, W

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations. by Gehmlich, K, Syrris, P, Peskett, E, Evans, A, Ehler, E, Asimaki, A, Anastasakis, A, Tsatsopoulou, A, Vouliotis, A, Stefanadis, C, Saffitz, J, Protonotarios, N, McKenna, W