OERTLI, Annemarie, RINNÉ, Susanne, MOSS, Kai Robin, KÄÄB, Stefan, SEEMANN, Gunnar, BECKMANN, Britt-Maria und DECHER, Niels, 2021. Molecular mechanism of autosomal eecessive long QT-syndrome 1 without deafness. Freiburg: Universität.
Elsevier - Harvard (with titles)Oertli, A., Rinné, S., Moss, K.R., Kääb, S., Seemann, G., Beckmann, B.-M., Decher, N., 2021. Molecular mechanism of autosomal eecessive long QT-syndrome 1 without deafness. Universität, Freiburg. https://doi.org/10.3390 jms22031112
American Psychological Association 7th editionOertli, A., Rinné, S., Moss, K. R., Kääb, S., Seemann, G., Beckmann, B.-M., & Decher, N. (ca. 2021). Molecular mechanism of autosomal eecessive long QT-syndrome 1 without deafness [Cd]. Universität. https://doi.org/10.3390 jms22031112
Springer - Basic (author-date)Oertli A, Rinné S, Moss KR, Kääb S, Seemann G, Beckmann B-M, Decher N (2021) Molecular mechanism of autosomal eecessive long QT-syndrome 1 without deafness. Universität, Freiburg
Juristische Zitierweise (Stüber) (Deutsch)Oertli, Annemarie/ Rinné, Susanne/ Moss, Kai Robin/ Kääb, Stefan/ Seemann, Gunnar/ Beckmann, Britt-Maria/ Decher, Niels, Molecular mechanism of autosomal eecessive long QT-syndrome 1 without deafness, Freiburg 2021.