Long QT syndrome-associated mutations in KCNQ1 and KCNE1 subunits disrupt normal endosomal recycling of IKs channels. [electronic resource]
Producer: 20090109Description: 1451-7 p. digitalISSN:- 1524-4571
- Animals
- COS Cells
- Chlorocebus aethiops
- Endosomes -- genetics
- Female
- KCNQ1 Potassium Channel -- genetics
- Long QT Syndrome -- genetics
- Mutation -- genetics
- Oocytes -- metabolism
- Potassium Channels, Inwardly Rectifying -- genetics
- Potassium Channels, Voltage-Gated -- genetics
- Protein Subunits -- genetics
- Xenopus Proteins -- genetics
- Xenopus laevis
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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