The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies. [electronic resource]
Producer: 20110114Description: E511-8 p. digitalISSN:- 1945-7197
- Adolescent
- Adult
- Bartter Syndrome -- drug therapy
- Child
- DNA Mutational Analysis
- Diuretics -- therapeutic use
- Exons -- genetics
- Female
- Frameshift Mutation
- Furosemide -- therapeutic use
- Gitelman Syndrome -- drug therapy
- Humans
- Male
- Mutation
- Receptors, Drug -- genetics
- Sequence Deletion -- genetics
- Sodium-Potassium-Chloride Symporters -- genetics
- Solute Carrier Family 12, Member 1
- Solute Carrier Family 12, Member 3
- Symporters -- genetics
- Thiazides -- therapeutic use
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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