Alqahtani, Y. A., Ghazali, B. M., Abbag, H. F., Abbag, W. F., Alghamdi, M. A., & Shati, S. A. (2022). A rare mutation in PRUNE 1- gene causing a neurodevelopmental disease with rare systemic manifestations in a Saudi child. International Journal of Health Sciences, 6(S5), 3968–3975. https://doi.org/10.53730/ijhs.v6nS5.9503