Valavi, E. and Fatahinezhad, E. 2023. Two non-familial cases of Galloway-Mowat syndrome carrying the homozygous mutations of WDR73 and TP53RK. Scientia Medica. 33, 1 (Oct. 2023), e44296. DOI:https://doi.org/10.15448/1980-6108.2023.1.44296.