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
Caner Alparslan 1 ,Elif Perihan Öncel 2 ,Sinem Akbay 3 ,Demet Alaygut 1 ,Fatma Mutlubaş 1 ,Mansur Tatlı 3 ,Martin Konrad 4 ,Önder Yavaşcan 1 ,Belde Kasap-Demir 1
1 Departments of Pediatric Nephrology, İzmir Tepecik Training and Research Hospital, , Izmir
2 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 :
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