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10.1253/circj.cj-23-0926
10.1253/circj.cj-23-0926
Towards a multidisciplinary approach of ECG screening in children and adolescents: a scoping review (2005-2025)
2025
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
2008
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No additional external references are available.