Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia

ConclusionsOur study shows that rare genetic mutations inPTGIR are enriched among FMD patients and found in SCAD patients, suggesting a role for prostacyclin signalling in non-atherosclerotic stenosis and dissection.
Source: Cardiovascular Research - Category: Cardiology Source Type: research