Hypercalciuria caused by CYP24A1 mutation: Fourteen years of the patient’s follow-up
Introduction. Recently, inactivation mutations of CYP24A1, the gene encoding vitamin D 24-hydroxylase, were identified in hypercalciuric nephrolithiasis and nephrocalcinosis. Here, we describe а long-term follow-up of a patient with hypercalciuric nephrolithiasis caused by CYP24A1 mutations. Case ou...
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| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Serbian Medical Society
2018-01-01
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| Seri Bilgileri: | Srpski Arhiv za Celokupno Lekarstvo |
| Konular: | |
| Online Erişim: | http://www.doiserbia.nb.rs/img/doi/0370-8179/2018/0370-81791700095P.pdf |
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