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Two Japanese Patients with Gitelman Syndrome
Gitelman syndrome (GS) is a renal tubular disorder characterized by hypokalemia, hypomagnesemia, metabolic alkalosis and hypocalciuria due to defective tubular reabsorption of magnesium and potassium. This disease is caused by mutations of the thiazide-sensitive Na-Cl cotransporter (NCCT) gene, SLC1...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The Japanese Society for Pediatric Endocrinology
2006
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4004865/ https://ncbi.nlm.nih.gov/pubmed/24790334 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.15.137 |
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