NICKEL, Kathrin Alexandra, TEBARTZ VAN ELST, Ludger, DOMSCHKE, Katharina, GLÄSER, Birgitta, STOCK, Friedrich, ENDRES, Dominique, MAIER, Simon und RIEDEL, Andreas, 2018. Heterozygous deletion of SCN2 A and SCN3 A in a patient with autism spectrum disorder and Tourette syndrome: a case report. Freiburg: Universität.
Elsevier - Harvard (with titles)Nickel, K.A., Tebartz van Elst, L., Domschke, K., Gläser, B., Stock, F., Endres, D., Maier, S., Riedel, A., 2018. Heterozygous deletion of SCN2 A and SCN3 A in a patient with autism spectrum disorder and Tourette syndrome: a case report. Universität, Freiburg. https://doi.org/10.1186/s12888-018-1822-8
American Psychological Association 7th editionNickel, K. A., Tebartz van Elst, L., Domschke, K., Gläser, B., Stock, F., Endres, D., Maier, S., & Riedel, A. (ca. 2018). Heterozygous deletion of SCN2 A and SCN3 A in a patient with autism spectrum disorder and Tourette syndrome: a case report [Cd]. Universität. https://doi.org/10.1186/s12888-018-1822-8
Springer - Basic (author-date)Nickel KA, Tebartz van Elst L, Domschke K, Gläser B, Stock F, Endres D, Maier S, Riedel A (2018) Heterozygous deletion of SCN2 A and SCN3 A in a patient with autism spectrum disorder and Tourette syndrome: a case report. Universität, Freiburg
Juristische Zitierweise (Stüber) (Deutsch)Nickel, Kathrin Alexandra/ Tebartz van Elst, Ludger/ Domschke, Katharina/ Gläser, Birgitta/ Stock, Friedrich/ Endres, Dominique/ Maier, Simon/ Riedel, Andreas, Heterozygous deletion of SCN2 A and SCN3 A in a patient with autism spectrum disorder and Tourette syndrome: a case report, Freiburg 2018.