Rare loss-of-function mutations of PTGIR identified in fibromuscular dysplasia and spontaneous coronary artery dissection
| Autor: | Georges, A., Albuisson, J., Berrandou, T., Dupré, D., Lorthioir, A., D’escamard, V., Warchoł-Celinska, E., Januszewicz, A., Bruneval, P., Baranowska, A.A., Adlam, D., Combaret, N., Motreff, P., Amar, L., Azizi, M., Gornik, H.L., Ganesh, S.K., Kovacic, J.L., Jeunemaitre, X., Bouatia-Naji, N. |
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| Zdroj: | In Archives of Cardiovascular Diseases Supplements October 2020 12(2-4):216-216 |
| Databáze: | ScienceDirect |
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