Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies.

MLA

Dworschak, Gabriel C., et al. “Biallelic and Monoallelic Variants in PLXNA1 Are Implicated in a Novel Neurodevelopmental Disorder with Variable Cerebral and Eye Anomalies.” Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 23, no. 9, Sept. 2021, pp. 1715–25. EBSCOhost, https://doi.org/10.1038/s41436-021-01196-9.

APA

Dworschak, G. C., Punetha, J., Kalanithy, J. C., Mingardo, E., Erdem, H. B., Akdemir, Z. C., Karaca, E., Mitani, T., Marafi, D., Fatih, J. M., Jhangiani, S. N., Hunter, J. V., Dakal, T. C., Dhabhai, B., Dabbagh, O., Alsaif, H. S., Alkuraya, F. S., Maroofian, R., Houlden, H., … Reutter, H. (2021). Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies. Genetics in Medicine : Official Journal of the American College of Medical Genetics, 23(9), 1715–1725. https://doi.org/10.1038/s41436-021-01196-9

Chicago

Dworschak, Gabriel C, Jaya Punetha, Jeshurun C Kalanithy, Enrico Mingardo, Haktan B Erdem, Zeynep C Akdemir, Ender Karaca, et al. 2021. “Biallelic and Monoallelic Variants in PLXNA1 Are Implicated in a Novel Neurodevelopmental Disorder with Variable Cerebral and Eye Anomalies.” Genetics in Medicine : Official Journal of the American College of Medical Genetics 23 (9): 1715–25. doi:10.1038/s41436-021-01196-9.