Delineating the GRIN1 phenotypic spectrum : A distinct genetic NMDA receptor encephalopathy

MLA

Lemke, Johannes R., et al. Delineating the GRIN1 Phenotypic Spectrum : A Distinct Genetic NMDA Receptor Encephalopathy. 2016. 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.on1303689495&authtype=sso&custid=ns315887.

APA

Lemke, J. R., Geider, K., Helbig, K. L., Heyne, H. O., Schütz, H., Hentschel, J., Courage, C., Depienne, C., Nava, C., Heron, D., Møller, R. S., Hjalgrim, H., Lal, D., Neubauer, B. A., Nürnberg, P., Thiele, H., Kurlemann, G., Arnold, G. L., Bhambhani, V., … Syrbe, S. (2016). Delineating the GRIN1 phenotypic spectrum : A distinct genetic NMDA receptor encephalopathy.

Chicago

Lemke, Johannes R., Kirsten Geider, Katherine L Helbig, Henrike O Heyne, Hannah Schütz, Julia Hentschel, Carolina Courage, et al. 2016. “Delineating the GRIN1 Phenotypic Spectrum : A Distinct Genetic NMDA Receptor Encephalopathy.” 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.on1303689495&authtype=sso&custid=ns315887.