@misc{indiciae96d579613811,
  title = {A point mutation in the nuclear speckle protein and splicing factor SRRM2 is associated with amyotrophic lateral sclerosis and causes dysregulation of synapse-associated genes},
  author = {Shi, Q. and Lauder, C. and Wang, Y.-D. and Elsakrmy, N. and Volkanoska, S. and Freibaum, B. D. and Peng, H. D. and Kim, H. J. and Taylor, J. P. and Cui, H.},
  year = {2025},
  doi = {10.1101/2025.09.11.675713},
  url = {https://www.biorxiv.org/content/10.1101/2025.09.11.675713v1},
  note = {Source identifier: 10.1101/2025.09.11.675713}
}