@misc{indiciae8eb8360683f9,
  title = {A homozygous variant in mitochondrial RNase P subunit PRORP is associated with Perrault syndrome characterized by hearing loss and primary ovarian insufficiency},
  author = {Hochberg, I. and Demain, L. A. M. and Urquhart, J. E. and Amberger, A. and Deutschmann, A. J. and Demetz, S. and Thompson, K. and O'Sullivan, J. and Belyantseva, I. A. and Barzik, M. and Williams, S. G. and Bhaskar, S. S. and Jenkinson, E. M. and AlSheqaih, N. and Blumenfeld, Z. and Yalonetsky, S. and Oerum, S. and Rossmanith, W. and Yue, W. W. and Zschocke, J. and Taylor, R. W. and Friedman, T. B. and Munro, K. J. and O'Keefe, R. T. and Newman, W. G.},
  year = {2017},
  doi = {10.1101/168252},
  url = {https://www.biorxiv.org/content/10.1101/168252v1},
  note = {Source identifier: 10.1101/168252}
}