Investigating a possible role of R3HCC1L in embryonic development and ocular disease
Megan C. Fischer, Linda M. Reis, Sanaa Muheisen, Sarah E. Seese, Elena V. Semina
The paper investigates R3HCC1L variants in a family with Peters anomaly and uses zebrafish models to assess its role in ocular development, finding no clear link to the phenotype.
bioRxiv · Oct 29, 2024 · PreprintGenetics