Reema AlGhofaili

A Novel GEMIN4 Variant in a Consanguineous Family Leads to Neurodevelopmental Impairment with Severe Microcephaly, Spastic Quadriplegia, Epilepsy, and Cataracts

S. Arold, N. Kaya, D. Çolak, 2021, Genes.

Clinical, radiological, and genetic characterization of SLC13A5 variants in Saudi families: Genotype phenotype correlation and brief review of the literature

N. Kaya, A. Alodaib, M. AlSayed, 2023, Frontiers in Pediatrics.