Cite
Screening of SLC2A1 in a large cohort of patients suspected for Glut1 deficiency syndrome: identification of novel variants and associated phenotypes
MLA
Castellotti, B., et al. Screening of SLC2A1 in a Large Cohort of Patients Suspected for Glut1 Deficiency Syndrome: Identification of Novel Variants and Associated Phenotypes. 2019. 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.on1308928898&authtype=sso&custid=ns315887.
APA
Castellotti, B., Ragona, F., Freri, E., Solazzi, R., Ciardullo, S., Tricomi, G., Venerando, A., Salis, B., Canafoglia, L., Villani, F., Franceschetti, S., Nardocci, N., Gellera, C., Difrancesco, J., Granata, T., Castellotti, B., Ragona, F., Freri, E., Solazzi, R., … Granata, T. (2019). Screening of SLC2A1 in a large cohort of patients suspected for Glut1 deficiency syndrome: identification of novel variants and associated phenotypes.
Chicago
Castellotti, B, F Ragona, E Freri, R Solazzi, S Ciardullo, G Tricomi, A Venerando, et al. 2019. “Screening of SLC2A1 in a Large Cohort of Patients Suspected for Glut1 Deficiency Syndrome: Identification of Novel Variants and Associated Phenotypes.” 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.on1308928898&authtype=sso&custid=ns315887.