@misc{indiciaec8743b205846,
  title = {Systematic re-annotation of 191 genes associated with early-onset epilepsy unmasks de novo variants linked to Dravet syndrome in novel SCN1A exons},
  author = {Steward, C. A. and Roovers, J. and Suner, M.-M. and Gonzalez, J.-M. and Uszczynska-Ratajczak, B. and Pervouchine, D. and Fitzgerald, S. and Margarida, V. and Samberger, H. and Hamdan, F. and Ceulemans, B. and Leroy, P. and Nava, C. and Lepine, A. and Tapanari, E. and Keiller, D. and Abbs, S. and Sanchis-Juan, A. and Grozeva, D. and Rogers, A. S. and Wright, J. and Choudhary, J. and Deikhans, M. and Guigo, R. and Petryszak, R. and Minassian, B. A. and Cavalleri, G. and Vistios, D. and Petrovski, S. and Harrow, J. and Flicek, P. and Raymond, F. L. and Lench, N. J. and De Jonghe, P. and Mudge, J. M. and Weckhuysen, S. and Sisodiya, S. M. and Frankish, A.},
  year = {2019},
  doi = {10.1101/648576},
  url = {https://www.biorxiv.org/content/10.1101/648576v1},
  note = {Source identifier: 10.1101/648576}
}