TY  - RPRT
TI  - 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
AU  - Shi, Q.
AU  - Lauder, C.
AU  - Wang, Y.-D.
AU  - Elsakrmy, N.
AU  - Volkanoska, S.
AU  - Freibaum, B. D.
AU  - Peng, H. D.
AU  - Kim, H. J.
AU  - Taylor, J. P.
AU  - Cui, H.
PY  - 2025
DO  - 10.1101/2025.09.11.675713
UR  - https://www.biorxiv.org/content/10.1101/2025.09.11.675713v1
ID  - 10.1101/2025.09.11.675713
ER  -