Whole-exome sequencing to identify causative variants in juvenile sudden cardiac death
Abstract Background Juvenile sudden cardiac death (SCD) remains unexplained in approximately 40% of cases, leading to a significant emotional burden for the victims’ families and society. Comprehensive investigations are essential to uncover its elusive causes and enable cascade family screening. Th...
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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMC
2024-09-01
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| Col·lecció: | Human Genomics |
| Matèries: | |
| Accés en línia: | https://doi.org/10.1186/s40246-024-00657-x |
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