Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndrome. [electronic resource]
Producer: 20140210Description: 3161-75 p. digitalISSN:- 1460-2075
- Action Potentials -- genetics
- Adult
- Cells, Cultured
- ERG1 Potassium Channel
- Embryonic Stem Cells -- physiology
- Ether-A-Go-Go Potassium Channels -- genetics
- Female
- Homeobox Protein Nkx-2.5
- Homeodomain Proteins -- genetics
- Humans
- Induced Pluripotent Stem Cells
- Long QT Syndrome -- genetics
- Mutation
- Myocytes, Cardiac -- pathology
- Patch-Clamp Techniques
- Phenotype
- Pluripotent Stem Cells -- physiology
- Protein Transport -- genetics
- Transcription Factors -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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