Defective protein trafficking in hERG-associated hereditary long QT syndrome (LQT2): molecular mechanisms and restoration of intracellular protein processing. [electronic resource]
Producer: 20040213Description: 235-41 p. digitalISSN:- 0008-6363
- Animals
- Cation Transport Proteins
- DNA-Binding Proteins
- ERG1 Potassium Channel
- Ether-A-Go-Go Potassium Channels
- Humans
- Intracellular Fluid -- metabolism
- Long QT Syndrome -- drug therapy
- Mutation
- Myocardium -- metabolism
- Potassium Channel Blockers -- therapeutic use
- Potassium Channels -- genetics
- Potassium Channels, Voltage-Gated
- Protein Transport
- Proteins -- metabolism
- Trans-Activators
- Transcriptional Regulator ERG
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
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