ALQAHTANI, Y. A.; GHAZALI, B. M.; ABBAG, H. F.; ABBAG, W. F.; ALGHAMDI, M. A.; SHATI, S. A. A rare mutation in PRUNE 1- gene causing a neurodevelopmental disease with rare systemic manifestations in a Saudi child. International journal of health sciences, [S. l.], v. 6, n. S5, p. 3968–3975, 2022. DOI: 10.53730/ijhs.v6nS5.9503. Disponível em: https://sciencescholar.us/journal/index.php/ijhs/article/view/9503. Acesso em: 10 jun. 2026.