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Bartter and Gitelman syndromes: Spectrum of clinical manifestations caused by different mutations
Bartter and Gitelman syndromes (BS and GS) are inherited disorders resulting in defects in renal tubular handling of sodium, potassium and chloride. Previously considered as genotypic and phenotypic heterogeneous diseases, recent evidence suggests that they constitute a spectrum of disease caused by...
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| Publicat a: | World J Methodol |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Baishideng Publishing Group Inc
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4482822/ https://ncbi.nlm.nih.gov/pubmed/26140272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5662/wjm.v5.i2.55 |
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