Fadie D Altuame

The natural history of infantile neuroaxonal dystrophy

F. Alkuraya, M. Salih, P. Atwal, 2019, Orphanet Journal of Rare Diseases.

PLXNA2 as a candidate gene in patients with intellectual disability

F. Alkuraya, N. Ewida, H. Shamseldin, 2021, American journal of medical genetics. Part A.