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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Circ Genom Precis Med |
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| Κύριοι συγγραφείς: | , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2019
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| Θέματα: | |
| Διαθέσιμο Online: | 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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