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A Practical Approach to Genetic Hypokalemia
Mutations in genes encoding ion channels, transporters, exchangers, and pumps in human tissues have been increasingly reported to cause hypokalemia. Assessment of history and blood pressure as well as the K(+) excretion rate and blood acid-base status can help differentiate between acquired and inhe...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
The Korean Society of Electrolyte Metabolism
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041498/ https://www.ncbi.nlm.nih.gov/pubmed/21468196 http://dx.doi.org/10.5049/EBP.2010.8.1.38 |