@misc{indiciaebdf78d8efafa,
  title = {Two therapeutic CRISPR/Cas9 gene editing approaches revert FTD/ALS cellular pathology caused by a C9orf72 repeat expansion mutation in patient derived cells},
  author = {Sckaff, M. and Gill, K. and Sachdev, A. and Birk, A. M. and Aladesuyi Arogundade, O. and Watry, H. L. and Keough, K. C. and Tsai, Y.-C. and Ziegle, J. and Conklin, B. R. and Clelland, C. D.},
  year = {2022},
  doi = {10.1101/2022.05.21.492887},
  url = {https://www.biorxiv.org/content/10.1101/2022.05.21.492887v1},
  note = {Source identifier: 10.1101/2022.05.21.492887}
}