Article Versions Notes

Brodehl A, Meshkov A, Myasnikov R, Kiseleva A, Kulikova O, Klauke B, Sotnikova E, Stanasiuk C, Divashuk M, Pohl GM, et al. Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset. International Journal of Molecular Sciences. 2021; 22(7):3786. https://doi.org/10.3390/ijms22073786

Brodehl, Andreas, Alexey Meshkov, Roman Myasnikov, Anna Kiseleva, Olga Kulikova, Bärbel Klauke, Evgeniia Sotnikova, Caroline Stanasiuk, Mikhail Divashuk, Greta Marie Pohl, and et al. 2021. "Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset" International Journal of Molecular Sciences 22, no. 7: 3786. https://doi.org/10.3390/ijms22073786

Brodehl, A., Meshkov, A., Myasnikov, R., Kiseleva, A., Kulikova, O., Klauke, B., Sotnikova, E., Stanasiuk, C., Divashuk, M., Pohl, G. M., Kudryavtseva, M., Klingel, K., Gerull, B., Zharikova, A., Gummert, J., Koretskiy, S., Schubert, S., Mershina, E., Gärtner, A., ... Milting, H. (2021). Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset. International Journal of Molecular Sciences, 22(7), 3786. https://doi.org/10.3390/ijms22073786