A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings

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YAVAŞCAN Ö.

TURKISH JOURNAL OF PEDIATRICS, vol.60, no.1, 2018 (SCI-Expanded)

• Publication Type: Article / Article
• Volume: 60 Issue: 1
• Publication Date: 2018
• Journal Name: TURKISH JOURNAL OF PEDIATRICS
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
• Istanbul Medipol University Affiliated: No