Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways

Rare familial spontaneous coronary artery dissection (SCAD) kindreds implicate genetic disease predisposition and provide a unique opportunity for candidate gene discovery. Whole-genome sequencing was performed in fifteen probands with non-syndromic SCAD who had a relative with SCAD, eight of whom h...

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Detalles Bibliográficos
Autores principales: Turley, Tamiel N., Theis, Jeanne L., Evans, Jared M., Fogarty, Zachary C., Gulati, Rajiv, Hayes, Sharonne N., Tweet, Marysia S., Olson, Timothy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532385/
https://www.ncbi.nlm.nih.gov/pubmed/37754822
http://dx.doi.org/10.3390/jcdd10090393

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532385/
https://www.ncbi.nlm.nih.gov/pubmed/37754822
http://dx.doi.org/10.3390/jcdd10090393

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