@misc{indiciae3e9832706120,
  title = {Mechanism-selective deep mutational scanning distinguishes ERCC2 disease phenotypes},
  author = {Cubuk, H. and Aslanzadeh, V. and Shang, Y. and Plech, M. and Pathak, A. and Kudla, G. and Marsh, J. A.},
  year = {2026},
  doi = {10.64898/2026.09.24.754105},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.24.754105v1},
  note = {Source identifier: 10.64898/2026.09.24.754105}
}