“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, vol. 23, no. G1, Sept. 2023, pp. 17-21, https://testing.journalofscience.org/index.php/GJSFR/article/view/102726.