Cite

    Brodehl, A., Weiss, J., Debus, J. D., Stanasiuk, C., Klauke, B., Deutsch, M. A., Fox, H., Bax, J., Ebbinghaus, H., Gärtner, A., Tiesmeier, J., Laser, T., Peterschröder, A., Gerull, B., Gummert, J., Paluszkiewicz, L., & Milting, H. (2020). a homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy. Journal of molecular and cellular cardiology, 141, 17–29. http://access.bl.uk/ark:/81055/vdc_100103931568.0x000053