@misc{indiciaea759d6734253,
  title = {Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy},
  author = {O'Donnell-Luria, A. H. and Pais, L. S. and Faundes, V. and Wood, J. C. and Sveden, A. and Luria, V. and Abou Jamra, R. and Accogli, A. and Amburgey, K. and Anderlid, B.-M. and Azzarello-Burri, S. and Basinger, A. A. and Bianchini, C. and Bird, L. M. and Buchert, R. and Carre, W. and Ceulemans, S. and Charles, P. and Cox, H. and Culliton, L. and Curro, A. and Deciphering Developmental Disorders (DDD) Study, and Demurger, F. and Dowling, J. J. and Duban-Bedu, B. and Dubourg, C. and Escobar, L. F. and Ferrarini, A. and Haack, T. B. and Hashim, M. and Heide, S. and Helbig, K. L. and Helbig, I. and Heredia, R. and Heron, D. and Isidor, B. and Jonasson, A. R. and Joset, P. and Keren, B. and Kok, F. and Kroes, H. Y},
  year = {2019},
  doi = {10.1101/566091},
  url = {https://www.biorxiv.org/content/10.1101/566091v1},
  note = {Source identifier: 10.1101/566091}
}