A Novel Bradycardia-Associated Variant in <i>HCN4</i> as a Candidate Modifier in Type 3 Long QT Syndrome: Case Report and Deep In Silico Analysis
<b>Background:</b> Genetic testing for long QT syndrome (LQTS) is straightforward in many families; however, in severe and complex cases, a single disease-causing variant may not be enough to explain all clinical features. In such cases, the search for genetic modifiers may be beneficial...
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| Main Authors: | , , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2025-04-01
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| Series: | Biomedicines |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2227-9059/13/4/1008 |
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