Heterozygous variants in KCNC2 cause a broad spectrum of epilepsy phenotypes associated with characteristic functional alterations 2021.05.21.21257099

MLA

Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group) [research center], et al. Heterozygous Variants in KCNC2 Cause a Broad Spectrum of Epilepsy Phenotypes Associated with Characteristic Functional Alterations 2021.05.21.21257099. 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.on1258960868&authtype=sso&custid=ns315887.

APA

Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group) [research center], BMBF Treat-ION grant (01GM1907). [sponsor], Schwarz, N., Seiffert, S., Pendziwiat, M., Rademacher, A., Brünger, T., Hedrich, U. B. S., Augustijn, P. B., Baier, H., Bayat, A., Bisulli, F., Buono, R. J., Bruria, B. Z., Doyle, M. G., Guerrini, R., Heimer, G., Iacomino, M., Kearney, H., … Weber, Y. (2021). Heterozygous variants in KCNC2 cause a broad spectrum of epilepsy phenotypes associated with characteristic functional alterations 2021.05.21.21257099.

Chicago

Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group) [research center], BMBF Treat-ION grant (01GM1907). [sponsor], Niklas Schwarz, Simone Seiffert, Manuela Pendziwiat, Annika Rademacher, Tobias Brünger, et al. 2021. “Heterozygous Variants in KCNC2 Cause a Broad Spectrum of Epilepsy Phenotypes Associated with Characteristic Functional Alterations 2021.05.21.21257099.” 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.on1258960868&authtype=sso&custid=ns315887.