Associated Papers
Talin-1 variants associated with spontaneous coronary artery dissection (SCAD) highlight how even subtle changes in multi-functional scaffold proteins can manifest in disease.
Azizi L et al.
Human Molecular Genetics, 2024
Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery Dissection.
Turley TN et al.
Circulation. Genomic and Precision Medicine, 2019
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