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Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes
BACKGROUND: Accurate interpretation of rare genetic variants is a challenge for clinical translation. Updates in recommendations for rare variant classification require the reanalysis and reclassification. We aim to perform an exhaustive re-analysis of rare variants associated with inherited arrhyth...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7136601/ https://www.ncbi.nlm.nih.gov/pubmed/32268277 http://dx.doi.org/10.1016/j.ebiom.2020.102732 |