@misc{indiciae4d7f252a1b10,
  title = {De novo heterozygous variants in EHMT2 genocopy Kleefstra syndrome via loss of G9a methyltransferase activity},
  author = {Hnizda, A. and Martinez-Delgado, B. and Sanchez-Ponce, D. and Alonso, J. and Amiel, J. and Attie-Bitach, T. and Bada-Navarro, A. and Baladron, B. and Bermejo-Sanchez, E. and Brinsa, V. and Bukova, I. and Cazorla-Calleja, R. and Cervenkova, S. and Chow, S. and Dusek, P. and Fernandez-Prieto, M. and Ghosh, S. and Gomez-Mariano, G. and Gregorova, A. and Hamilton, M. J. and Hartmannova, H. and Hernandez-San Miguel, E. and Herrero-Matesanz, M. and Hodanova, K. and Kadek, A. and Kerkhof, J. and Kleefstra, T. and Lacombe, D. and Levy, M. A. and Lopez-Martin, E. and Lyse, R. and Man, P. and Marin-Reina, P. and Macnamara, E. F. and McConkey, H. and Melenovska, P. and Mielu, L. M. and Moore, D. and Mrazova, L. and Mus},
  year = {2025},
  doi = {10.1101/2025.09.25.678439},
  url = {https://www.biorxiv.org/content/10.1101/2025.09.25.678439v1},
  note = {Source identifier: 10.1101/2025.09.25.678439}
}