Cite
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. 2021. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1312208308&authtype=sso&custid=ns315887.
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.
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.” http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1312208308&authtype=sso&custid=ns315887.