1.
Whole Exome Sequencing Identifies a Novel Mutation in ADGRV1 Responsible For Usher 2C Syndrome in a Large Inbred Family. GJSFR. 2023;23(G1):17-21. Accessed February 5, 2026. https://www.journalofscience.org/index.php/GJSFR/article/view/102726