2 Publikationen
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916928Schirmer, I.; Dieding, M.; Klauke, B.; Brodehl, A.; Gärtner-Rommel, A.; Walhorn, V.; Gummert, J.; Schulz, U.; Paluszkiewicz, L.; Anselmetti, D.; Milting, H. (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): 288-293.PUB | DOI | Download (ext.) | WoS | PubMed | Europe PMC
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2915089Dieding, M.; Debus, J. D.; Kerkhoff, R.; Gärtner-Rommel, A.; Walhorn, V.; Milting, H.; Anselmetti, D. (2017): Arrhythmogenic cardiomyopathy related DSG2 mutations affect desmosomal cadherin binding kinetics Scientific Reports,7:(1):13791PUB | DOI | WoS | PubMed | Europe PMC