@misc{indiciaeb3ad281d7385,
  title = {Bi-allelic variants in WDR47 lead to neuronal loss causing a rare neurodevelopmental syndrome with corpus callosum dysgenesis in humans.},
  author = {Bayam, E. and Tilly, P. and Collins, S. and Rivera Alvarez, J. and Kannan, M. and Tonneau, L. and Rinaldi, B. and Lecat, R. and Schwaller, N. and Maddirevula, S. and Monteiro, F. and Kitajima, J. P. and Kok, F. and Kato, M. and Hamed, A. A. A. and Salih, M. A. and Al Tala, S. and O Hashem, M. and Tada, H. and Saitsu, H. and Friant, S. and Yüksel, Z. and Nakashima, M. and Alkuraya, F. S. and Yalcin, B. and GODIN, J. D.},
  year = {2023},
  doi = {10.1101/2023.12.22.572779},
  url = {https://www.biorxiv.org/content/10.1101/2023.12.22.572779v1},
  note = {Source identifier: 10.1101/2023.12.22.572779}
}