Whole Exome Sequencing Identifies a Novel Mutation in ADGRV1 Responsible For Usher 2C Syndrome in a Large Inbred Family. Global Journal of Science Frontier Research, [S. l.], v. 23, n. G1, p. 17–21, 2023. Disponível em: https://testing.journalofscience.org/index.php/GJSFR/article/view/102726. Acesso em: 4 feb. 2026.