GeneticsbioRxivPreprint
Investigating a possible role of R3HCC1L in embryonic development and ocular disease
Megan C. Fischer, Linda M. Reis, Sanaa Muheisen…·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.
DOI 10.1101/2024.10.29.620958