2 Publikationen
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916928I. Schirmer, et al., “A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy”, Molecular Genetics & Genomic Medicine, vol. 6, 2018, pp. 288-293.PUB | DOI | Download (ext.) | WoS | PubMed | Europe PMC
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2915089M. Dieding, et al., “Arrhythmogenic cardiomyopathy related DSG2 mutations affect desmosomal cadherin binding kinetics”, Scientific Reports, vol. 7, 2017, : 13791.PUB | DOI | WoS | PubMed | Europe PMC