Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome. [electronic resource]
Producer: 19961230Description: 13200-5 p. digitalISSN:- 0027-8424
- Animals
- Base Sequence
- Cell Line
- Cloning, Molecular
- DNA Primers
- Heart -- physiology
- Humans
- Kidney
- Kinetics
- Long QT Syndrome -- genetics
- Mammals
- Membrane Potentials
- Muscular Diseases -- physiopathology
- Mutagenesis, Site-Directed
- NAV1.5 Voltage-Gated Sodium Channel
- Oligodeoxyribonucleotides
- Patch-Clamp Techniques
- Point Mutation
- Polymerase Chain Reaction
- Recombinant Proteins -- biosynthesis
- Sodium Channels -- genetics
- Transfection
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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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