2 Publikationen
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916928Schirmer, I., et al., 2018. A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy. Molecular Genetics & Genomic Medicine, 6(2), p 288-293.PUB | DOI | Download (ext.) | WoS | PubMed | Europe PMC
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2915089Dieding, M., et al., 2017. Arrhythmogenic cardiomyopathy related DSG2 mutations affect desmosomal cadherin binding kinetics. Scientific Reports, 7(1): 13791.PUB | DOI | WoS | PubMed | Europe PMC