JUAN CARLOS KUAN; MARIA ALEXANDRA ANGEL; JUAN PABLO BERNAL; MARÍA TERESA PIÑEROS; MARÍA TERESA PIÑEROS. 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://journalofscience.org/index.php/GJSFR/article/view/102726. Acesso em: 15 jan. 2025.