OERTLI, Annemarie, RINNÉ, Susanne, MOSS, Kai Robin, KÄÄB, Stefan, SEEMANN, Gunnar, BECKMANN, Britt-Maria und DECHER, Niels, [no date]. Molecular mechanism of autosomal recessive long QT-syndrome 1 without deafness. International journal of molecular sciences. No. Band 22 (2021), Seite 1-13, Artikel-ID: 1112, p. , Seite 1-13, Artikel. DOI 10.3390 jms22031112.
Elsevier - Harvard (with titles)Oertli, A., Rinné, S., Moss, K.R., Kääb, S., Seemann, G., Beckmann, B.-M., Decher, N., o. J. Molecular mechanism of autosomal recessive long QT-syndrome 1 without deafness. International journal of molecular sciences , Seite 1-13, Artikel. 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. (o. J.). Molecular mechanism of autosomal recessive long QT-syndrome 1 without deafness [Electronic]. International journal of molecular sciences, Band 22 (2021), Seite 1-13, Artikel-ID: 1112, , Seite 1-13, Artikel. 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 Molecular mechanism of autosomal recessive long QT-syndrome 1 without deafness. International journal of molecular sciences , Seite 1-13, Artikel. https://doi.org/10.3390 jms22031112
Juristische Zitierweise (Stüber) (Deutsch)Oertli, Annemarie/ Rinné, Susanne/ Moss, Kai Robin/ Kääb, Stefan/ Seemann, Gunnar/ Beckmann, Britt-Maria/ Decher, Niels, Molecular mechanism of autosomal recessive long QT-syndrome 1 without deafness, International journal of molecular sciences , , Seite 1-13, Artikel.