Rare Missense Variants in TLN1 Are Associated with Familial and Sporadic Spontaneous Coronary Artery Dissection

BACKGROUND: Spontaneous coronary artery dissection (SCAD) is an uncommon idiopathic disorder predominantly affecting young, otherwise healthy women. Rare familial cases reveal a genetic predisposition to disease. The aim of this study was to identify a novel susceptibility gene for SCAD. METHODS: Wh...

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Publicat a:Circ Genom Precis Med
Autors principals: Turley, Tamiel N., Theis, Jeanne L., Sundsbak, Rhianna S., Evans, Jared M., O’Byrne, Megan M., Gulati, Rajiv, Tweet, Marysia S., Hayes, Sharonne N., Olson, Timothy M.
Format: Artigo
Idioma:Inglês
Publicat: 2019
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6625931/
https://ncbi.nlm.nih.gov/pubmed/30888838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGEN.118.002437
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