Systematic re-annotation of 191 genes associated with early-onset epilepsy unmasks de novo variants linked to Dravet syndrome in novel SCN1A exons

MLA

Stephen Abbs, et al. Systematic Re-Annotation of 191 Genes Associated with Early-Onset Epilepsy Unmasks de Novo Variants Linked to Dravet Syndrome in Novel SCN1A Exons. May 2019. EBSCOhost, https://doi.org/10.1101/648576.

APA

Stephen Abbs, Caroline Nava, Sanjay M. Sisodiya, Jyoti S. Choudhary, Dimitrios Vitsios, Dmitri D. Pervouchine, Electra Tapanari, Fadi F. Hamdan, Hannah Stamberger, Berten Ceulemans, Detelina Grozeva, Jennifer Harrow, Patricia Leroy, Marie Marthe Suner, Charles A. Steward, Gianpiero L. Cavalleri, Margarida Viola, Anne Fabienne Lepine, José M. González, … Berge A. Minassian. (2019). Systematic re-annotation of 191 genes associated with early-onset epilepsy unmasks de novo variants linked to Dravet syndrome in novel SCN1A exons. https://doi.org/10.1101/648576

Chicago

Stephen Abbs, Caroline Nava, Sanjay M. Sisodiya, Jyoti S. Choudhary, Dimitrios Vitsios, Dmitri D. Pervouchine, Electra Tapanari, et al. 2019. “Systematic Re-Annotation of 191 Genes Associated with Early-Onset Epilepsy Unmasks de Novo Variants Linked to Dravet Syndrome in Novel SCN1A Exons,” May. doi:10.1101/648576.