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HERG, a Human Inward Rectifier in the Voltage-Gated Potassium Channel Family
Abstract
In contrast to other members of the Eag family of voltage-gated, outwardly rectifying potassium channels, the human eag -related gene ( HERG ) has now been shown to encode an inwardly rectifying potassium channel. The properties of HERG channels are consistent with the gating properties of Eag-related and other outwardly rectifying, S4-containing potassium channels, but with the addition of an inactivation mechanism that attenuates potassium efflux during depolarization. Because mutations in HERG cause a form of long-QT syndrome, these properties of HERG channel function may be critical to the maintenance of normal cardiac rhythmicity.
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Metadata
- Authors
- Trudeau, M. C., Warmke, J. W., Ganetzky, B., & Robertson, G. A.
- Venue
- Science
- Published
- 1995-07-07
- Volume
- 269
- Issue
- 5220
- Pages
- 92-95
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2021438486
- Cited by
- 1,239
- References
- 0
- FWCI
- 16.11
- Type
- journal article
- Language
- en
- Open access
- closed
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