Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions

MLA

Simon Pope, et al. Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions. 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=edsair&AN=edsair.doi.dedup.....d0afa00c777f2324cecaedd0d6450b6c&authtype=sso&custid=ns315887. Accessed 2 Feb. 2025.

APA

Simon Pope, Lillian Martinian, Krishna Chinthapalli, Claudia B. Catarino, Shazia Adalat, John S. Duncan, Martin Koltzenburg, Detlef Bockenhauer, Hannah Cohen, Lisa M. S. Clayton, Dalia Kasperavičiūtė, Maria Thom, Peter Hammond, Sanjay M. Sisodiya, John M. Land, Nicholas Lench, & Raoul C.M. Hennekam. (n.d.). Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions.

Chicago

Simon Pope, Lillian Martinian, Krishna Chinthapalli, Claudia B. Catarino, Shazia Adalat, John S. Duncan, Martin Koltzenburg, et al. 2025. “Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions.” Accessed February 2. 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=edsair&AN=edsair.doi.dedup.....d0afa00c777f2324cecaedd0d6450b6c&authtype=sso&custid=ns315887.