APA (7th ed.) Citation

Semino, F., Schröter, J., Willemsen, M. H., Bast, T., Biskup, S., Beck-Woedl, S., . . . Syrbe, S. (2021). Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder. Human mutation, 42(9), . https://doi.org/10.1002/humu.24245

Chicago Style (17th ed.) Citation

Semino, Francesca, et al. "Further Evidence for De Novo Variants in SYNCRIP as the Cause of a Neurodevelopmental Disorder." Human Mutation 42, no. 9 (2021). https://doi.org/10.1002/humu.24245.

MLA (9th ed.) Citation

Semino, Francesca, et al. "Further Evidence for De Novo Variants in SYNCRIP as the Cause of a Neurodevelopmental Disorder." Human Mutation, vol. 42, no. 9, 2021, https://doi.org/10.1002/humu.24245.