Georges, A., Albuisson, J., Berrandou, T., Dupré, D., Lorthioir, A., D'Escamard, V., Di Narzo, A. F., Kadian-Dodov, D., Olin, J. W., Warchol-Celinska, E., Prejbisz, A., Januszewicz, A., Bruneval, P., Baranowska, A. A., Webb, T. R., Hamby, S. E., Samani, N. J., Adlam, D., Fendrikova-Mahlay, N., Hazen, S., Wang, Y., Yang, M., Hunker, K., Combaret, N., Motreff, P., Chédid, A., Fiquet, B., Plouin, P., Mousseaux, E., Azarine, A., Amar, L., Azizi, M., Gornik, H. L., Ganesh, S. K., Kovacic, J. C., Jeunemaitre, X., & Bouatia-Naji, N. (2021). rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia. Cardiovascular research, 117(4), 1154–1165. http://access.bl.uk/ark:/81055/vdc_100123430645.0x00004f