Gene-therapy in inherited channelopathies like short-QT syndrome: a robust direction towards precision medicine
This editorial refers to ‘AAV9-mediated KCNH2 suppression-replacement gene therapy in a transgenic rabbit model of type 1 short QT syndrome’, by S. Nimani et al., https://doi.org/10.1093/eurheartj/ehaf660.Short-QT Syndrome (SQTS) is an inherited channelopathy first described two decades ago. This di...
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| Main Authors: | , , |
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| Format: | Article (Journal) Editorial |
| Language: | English |
| Published: |
7 January 2026
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| In: |
European heart journal
Year: 2026, Volume: 47, Issue: 2, Pages: 214-216 |
| ISSN: | 1522-9645 |
| DOI: | 10.1093/eurheartj/ehaf831 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1093/eurheartj/ehaf831
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| Author Notes: | Nazha Hamdani, Ibrahim Akin, and Ibrahim El-Battrawy |
| Summary: | This editorial refers to ‘AAV9-mediated KCNH2 suppression-replacement gene therapy in a transgenic rabbit model of type 1 short QT syndrome’, by S. Nimani et al., https://doi.org/10.1093/eurheartj/ehaf660.Short-QT Syndrome (SQTS) is an inherited channelopathy first described two decades ago. This disorder is associated with sudden cardiac death, atrial fibrillation, and bradycardia occurring in childhood |
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| Item Description: | Gesehen am 12.01.2026 |
| Physical Description: | Online Resource |
| ISSN: | 1522-9645 |
| DOI: | 10.1093/eurheartj/ehaf831 |