Whole Exome Sequencing Identifies a Novel Mutation in ADGRV1 Responsible For Usher 2C Syndrome in a Large Inbred Family. GJSFR [Internet]. 2023 Sep. 28 [cited 2026 Feb. 4];23(G1):17-21. Available from: https://testing.journalofscience.org/index.php/GJSFR/article/view/102726