Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. [electronic resource]
Producer: 19960201Description: 17-23 p. digitalISSN:- 1061-4036
- Amino Acid Sequence
- Base Sequence
- Chromosomes, Human, Pair 11
- Cloning, Molecular
- Female
- Genetic Linkage
- Humans
- Long QT Syndrome -- genetics
- Male
- Molecular Sequence Data
- Pedigree
- Point Mutation
- Polymorphism, Single-Stranded Conformational
- Potassium Channels -- genetics
- Sequence Alignment
- Sequence Deletion
- Sequence Homology, Amino Acid
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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