Chloride channels in renal disease.
Recent studies of hereditary renal tubular disorders have facilitated the identification and roles of chloride channels and cotransporters in the regulation of the most abundant anion, Cl-, in the ECF. Thus, mutations that result in a loss of function of the voltage-gated chloride channel, CLC-5, ar...
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| フォーマット: | Journal article |
| 言語: | English |
| 出版事項: |
1999
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