A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings.
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M. Konrad | D. Alaygut | F. Mutlubaş | Belde Kasap-Demir | C. Alparslan | S. Akbay | Ö. Yavaşcan | E. Öncel | M. Tatli
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