@misc{indiciae2f4e16b08f8c,
  title = {CBX1 mutations cause a neurodevelopmental syndrome due to heterochromatin organizational alterations},
  author = {Iwata-Otsubo, A. and Lindsay-Temple, S. and Dias, K.-R. and Zhu, Y. and Fiordaliso, S. and Su, C. and Ritter, A. and Baker, S. W. and Kuroda, Y. and Keena, B. A. and Grant, S. F. and Zackai, E. and Edwards, M. and Evans, C.-A. and Dulik, M. C. and Buckley, M. F. and Roscioli, T. and Izumi, K.},
  year = {2020},
  doi = {10.1101/2020.09.29.319228},
  url = {https://www.biorxiv.org/content/10.1101/2020.09.29.319228v1},
  note = {Source identifier: 10.1101/2020.09.29.319228}
}