@misc{indiciae4f48d1090eff,
  title = {A novel de novo FEM1C variant as a potential cause of neurodevelopmental disorder with absent speech, pyramidal signs, and limb ataxia.},
  author = {Dubey, A. A. and Krygier, M. and Szulc, N. A. and Rutkowska, K. and Kosinska, J. and Pollak, A. and Rydzanicz, M. and Kmiec, T. and Mazurkiewicz-Beldzinska, M. and Pokrzywa, W. and Ploski, R.},
  year = {2022},
  doi = {10.1101/2022.04.24.489208},
  url = {https://www.biorxiv.org/content/10.1101/2022.04.24.489208v1},
  note = {Source identifier: 10.1101/2022.04.24.489208}
}