APA (7th ed.) Citation

Dafsari, H. S., Sprute, R., Wunderlich, G., Daimagüler, H., Karaca, E., Contreras, A., . . . Cirak, S. (2019). Correction to: Novel mutations in KMT2B offer pathophysiological insights on childhood-onset progressive dystonia. Journal of human genetics, 64(10), . https://doi.org/10.1038/s10038-019-0644-y

Chicago Style (17th ed.) Citation

Dafsari, Hormos Salimi, et al. "Correction to: Novel Mutations in KMT2B Offer Pathophysiological Insights on Childhood-onset Progressive Dystonia." Journal of Human Genetics 64, no. 10 (2019). https://doi.org/10.1038/s10038-019-0644-y.

MLA (9th ed.) Citation

Dafsari, Hormos Salimi, et al. "Correction to: Novel Mutations in KMT2B Offer Pathophysiological Insights on Childhood-onset Progressive Dystonia." Journal of Human Genetics, vol. 64, no. 10, 2019, https://doi.org/10.1038/s10038-019-0644-y.