Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current. [electronic resource]
Producer: 20100107Description: 667-76 p. digitalISSN:- 1941-3084
- Animals
- Calcium-Binding Proteins -- genetics
- Cell Line
- DNA Mutational Analysis
- Enzyme Inhibitors -- pharmacology
- Female
- Genotype
- Humans
- Infant
- Infant, Newborn
- Ion Channel Gating
- Long QT Syndrome -- genetics
- Male
- Membrane Potentials
- Membrane Proteins -- genetics
- Mice
- Muscle Proteins -- drug effects
- Mutation, Missense
- Myocardium -- metabolism
- NAV1.5 Voltage-Gated Sodium Channel
- Nitric Oxide Synthase -- antagonists & inhibitors
- Nitric Oxide Synthase Type I
- Open Reading Frames
- Patch-Clamp Techniques
- Phenotype
- Plasma Membrane Calcium-Transporting ATPases -- metabolism
- Rats
- Sodium -- metabolism
- Sodium Channels -- drug effects
- Sudden Infant Death -- genetics
- Time Factors
- Transfection
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.