APA citiranje

Fatima, A., Hoeber, J., Schuster, J., Koshimizu, E., Maya-Gonzalez, C., Keren, B., . . . Dahl, N. (2021). Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy. Am J Hum Genet.

Citação norma Chicago

Fatima, Ambrin, et al. "Monoallelic and Bi-allelic Variants in NCDN Cause Neurodevelopmental Delay, Intellectual Disability, and Epilepsy." Am J Hum Genet 2021.

MLA citiranje

Fatima, Ambrin, et al. "Monoallelic and Bi-allelic Variants in NCDN Cause Neurodevelopmental Delay, Intellectual Disability, and Epilepsy." Am J Hum Genet 2021.