Genetic forms of renal potassium and magnesium wasting. [electronic resource]
Producer: 20020327Description: 235-6 p. digitalISSN:- 0002-9343
- Bartter Syndrome -- genetics
- Carrier Proteins -- genetics
- Genotype
- Humans
- Hypokalemia -- genetics
- Magnesium Deficiency -- genetics
- Mutation
- Phenotype
- Potassium Channels -- genetics
- Potassium Channels, Inwardly Rectifying
- Receptors, Drug
- Renal Tubular Transport, Inborn Errors -- genetics
- Sodium Chloride Symporters
- Sodium-Potassium-Chloride Symporters -- genetics
- Solute Carrier Family 12, Member 1
- Solute Carrier Family 12, Member 3
- Symporters
No physical items for this record
Publication Type: Comment; Editorial
There are no comments on this title.
Log in to your account to post a comment.