Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK. [electronic resource]
Producer: 19961112Description: 152-6 p. digitalISSN:- 1061-4036
- Amino Acid Sequence
- Bartter Syndrome -- genetics
- Carrier Proteins -- genetics
- Cell Membrane -- chemistry
- Consanguinity
- Conserved Sequence
- DNA Mutational Analysis
- Female
- Genetic Heterogeneity
- Genotype
- Humans
- Male
- Mutation
- Pedigree
- Polymorphism, Single-Stranded Conformational
- Potassium Channels -- chemistry
- Potassium Channels, Inwardly Rectifying
- Sodium-Potassium-Chloride Symporters
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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