2 Publikationen
-
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916928PUB | DOI | Download (ext.) | WoS | PubMed | Europe PMCSchirmer, 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. Wiley-Blackwell. doi:10.1002/mgg3.358.
-
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2915089PUB | DOI | WoS | PubMed | Europe PMCDieding, 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): 13791. Nature Publishing Group. doi:10.1038/s41598-017-13737-x.