2 Publikationen
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916928A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathyPUB | DOI | Download (ext.) | WoS | PubMed | Europe PMC
Schirmer I, Dieding M, Klauke B, Brodehl A, Gärtner-Rommel A, Walhorn V, Gummert J, Schulz U, Paluszkiewicz L, Anselmetti D, Milting H (2018)
Molecular Genetics & Genomic Medicine 6(2): 288-293. -
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2915089Arrhythmogenic cardiomyopathy related DSG2 mutations affect desmosomal cadherin binding kineticsPUB | DOI | WoS | PubMed | Europe PMC
Dieding M, Debus JD, Kerkhoff R, Gärtner-Rommel A, Walhorn V, Milting H, Anselmetti D (2017)
Scientific Reports 7(1): 13791.