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.: A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy. Molecular Genetics & Genomic Medicine. 6, 288-293 (2018).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.: Arrhythmogenic cardiomyopathy related DSG2 mutations affect desmosomal cadherin binding kinetics. Scientific Reports. 7, : 13791 (2017).PUB | DOI | WoS | PubMed | Europe PMC