Article Versions Notes

Brodehl A, Hain C, Flottmann F, Ratnavadivel S, Gaertner A, Klauke B, Kalinowski J, Körperich H, Gummert J, Paluszkiewicz L, et al. The Desmin Mutation DES-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3. Biomedicines. 2021; 9(10):1400. https://doi.org/10.3390/biomedicines9101400

Brodehl, Andreas, Carsten Hain, Franziska Flottmann, Sandra Ratnavadivel, Anna Gaertner, Bärbel Klauke, Jörn Kalinowski, Hermann Körperich, Jan Gummert, Lech Paluszkiewicz, and et al. 2021. "The Desmin Mutation DES-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3" Biomedicines 9, no. 10: 1400. https://doi.org/10.3390/biomedicines9101400

Brodehl, A., Hain, C., Flottmann, F., Ratnavadivel, S., Gaertner, A., Klauke, B., Kalinowski, J., Körperich, H., Gummert, J., Paluszkiewicz, L., Deutsch, M.-A., & Milting, H. (2021). The Desmin Mutation DES-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3. Biomedicines, 9(10), 1400. https://doi.org/10.3390/biomedicines9101400