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

MLA

Dalia Kasperavičiūtė, et al. “Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions.” PLoS ONE, vol. 6, no. 8, Jan. 2011, p. e23182. EBSCOhost, https://doi.org/10.1371/journal.pone.0023182.

APA

Dalia Kasperavičiūtė, Claudia B Catarino, Krishna Chinthapalli, Lisa M S Clayton, Maria Thom, Lillian Martinian, Hannah Cohen, Shazia Adalat, Detlef Bockenhauer, Simon A Pope, Nicholas Lench, Martin Koltzenburg, John S Duncan, Peter Hammond, Raoul C M Hennekam, John M Land, & Sanjay M Sisodiya. (2011). Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions. PLoS ONE, 6(8), e23182. https://doi.org/10.1371/journal.pone.0023182

Chicago

Dalia Kasperavičiūtė, Claudia B Catarino, Krishna Chinthapalli, Lisa M S Clayton, Maria Thom, Lillian Martinian, Hannah Cohen, et al. 2011. “Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions.” PLoS ONE 6 (8): e23182. doi:10.1371/journal.pone.0023182.