Özgün, N. and Merve Saka Güvenç, M. 2025. Rafiq Syndrome: Old Variant in MAN1B1 Gene and Some New Phenotypic Features. Iranian Journal of Child Neurology. 19, 1 (Jan. 2025), 121–126. DOI:https://doi.org/10.22037/ijcn.v19i1.42376.