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Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples
Molecular screening for pathogenic mutations in sudden cardiac death (SCD)-related genes is common practice for SCD cases. However, test results may lead to uncertainty because of the identification of variants of unknown significance (VUS) occurring in up to 70% of total identified variants due to...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604081/ https://www.ncbi.nlm.nih.gov/pubmed/36293497 http://dx.doi.org/10.3390/ijms232012640 |