FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects

MLA

Generalitat de Catalunya, et al. FOSL2 Truncating Variants in the Last Exon Cause a Neurodevelopmental Disorder with Scalp and Enamel Defects. 2022. 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.on1373158307&authtype=sso&custid=ns315887.

APA

Generalitat de Catalunya, Cospain, A., Rivera-Barahona, A., Dumontet, E., Gener, B., Bailleul-Forestier, I., Meyts, I., Jouret, G., Isidor, B., Brewer, C., Wuyts, W., Moens, L., Delafontaine, S., Wing Keung Lam, W., Van Den Bogaert, K., Boogaerts, A., Scalais, E., Besnard, T., Cogne, B., … Pérez-Jurado, L. A. (2022). FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects.

Chicago

Generalitat de Catalunya, Auriane Cospain, Ana Rivera-Barahona, Erwan Dumontet, Blanca Gener, Isabelle Bailleul-Forestier, Isabelle Meyts, et al. 2022. “FOSL2 Truncating Variants in the Last Exon Cause a Neurodevelopmental Disorder with Scalp and Enamel Defects.” 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.on1373158307&authtype=sso&custid=ns315887.