The Turkish Journal of Pediatrics
2018 , Vol 60 , Num 1
A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings
1 Departments of Pediatric Nephrology, İzmir Tepecik Training and Research Hospital, , Izmir2 Departments of Pediatrics, İzmir Tepecik Training and Research Hospital
3 Departments of Neonatal Intensive Care Unit, İzmir Katip Çelebi University, Izmir
4 Department of General Pediatrics, University Children’s Hospital, Münster, Germany
5 Departments of Pediatric Nephrology İzmir Katip Çelebi University, Izmir DOI : 10.24953/turkjped.2018.01.011 Keywords :