@misc{indiciae630e8af13e9d,
  title = {Whole genome sequencing for diagnosis of neurological repeat expansion disorders},
  author = {Ibanez, K. and Polke, J. and Hagelstrom, T. and Dolzhenko, E. and Pasko, D. and Thomas, E. and Daugherty, L. and Kasperaviciute, D. and McDonagh, E. M. and Smith, K. R. and Rueda Martin, A. and Polychronopoulos, D. and Angus-Leppan, H. and Bhatia, K. P. and Davison, J. E. and Festenstein, R. and Fratta, P. and Giunti, P. and Howard, R. and Korlipara, L. V. P. and Laura, M. and McEntagart, M. and Menzies, L. and Morris, H. and Reilly, M. M. and Robinson, R. and Rosser, E. and Faravelli, F. and Schrag, A. and Schott, J. M. and Warner, T. T. and Wood, N. W. and Bourn, D. and Eggleton, K. and Labrum, R. and Twiss, P. and Abbs, S. and Santos, L. and Almheiri, G. and Sheikh, I. and Vandrovcova, J. and Patch, C. and Tavares},
  year = {2020},
  doi = {10.1101/2020.11.06.371716},
  url = {https://www.biorxiv.org/content/10.1101/2020.11.06.371716v1},
  note = {Source identifier: 10.1101/2020.11.06.371716}
}