Alqahtani, Y.A., Ghazali, B.M., Abbag, H.F., Abbag, W.F., Alghamdi, M.A. and 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 (Jun. 2022), 3968–3975. DOI:https://doi.org/10.53730/ijhs.v6nS5.9503.