Determining the Likelihood of Disease Pathogenicity Among Incidentally Identified Genetic Variants in Rare Dilated Cardiomyopathy‐Associated Genes

BACKGROUND: As utilization of clinical exome sequencing (ES) has expanded, criteria for evaluating the diagnostic weight of incidentally identified variants are critical to guide clinicians and researchers. This is particularly important in genes associated with dilated cardiomyopathy (DCM), which c...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Qixin, Berkman, Amy M., Ezekian, Jordan E., Rosamilia, Michael, Rosenfeld, Jill A., Liu, Pengfei, Landstrom, Andrew P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673717/
https://www.ncbi.nlm.nih.gov/pubmed/36129056
http://dx.doi.org/10.1161/JAHA.122.025257

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673717/
https://www.ncbi.nlm.nih.gov/pubmed/36129056
http://dx.doi.org/10.1161/JAHA.122.025257

Ejemplares similares