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

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