1.
Alqahtani YA, Ghazali BM, Abbag HF, Abbag WF, Alghamdi MA, Shati SA. A rare mutation in PRUNE 1- gene causing a neurodevelopmental disease with rare systemic manifestations in a Saudi child. Int. J. of Health Sci. [Internet]. 2022 Jun. 23 [cited 2026 May 19];6(S5):3968-75. Available from: https://sciencescholar.us/journal/index.php/ijhs/article/view/9503