APA-Zitierstil (7. Ausg.)

Dafsari, H. S., Sprute, R., Wunderlich, G., Daimagüler, H., Karaca, E., Contreras, A., . . . Cirak, S. (2019). Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia. Journal of human genetics, 64(8), . https://doi.org/10.1038/s10038-019-0625-1

Chicago-Zitierstil (17. Ausg.)

Dafsari, Hormos Salimi, et al. "Novel Mutations in KMT2B Offer Pathophysiological Insights into Childhood-onset Progressive Dystonia." Journal of Human Genetics 64, no. 8 (2019). https://doi.org/10.1038/s10038-019-0625-1.

MLA-Zitierstil (9. Ausg.)

Dafsari, Hormos Salimi, et al. "Novel Mutations in KMT2B Offer Pathophysiological Insights into Childhood-onset Progressive Dystonia." Journal of Human Genetics, vol. 64, no. 8, 2019, https://doi.org/10.1038/s10038-019-0625-1.