학술논문
Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia
Document Type
Article
Author
Georges, A.; Albuisson, J.; Berrandou, T.; Dupré, D.; Bruneval, P.; Mousseaux, E.; Amar, L.; Jeunemaitre, X.; Bouatia-Naji, N.; Lorthioir, A.; Chédid, A.; Fiquet, B.; Plouin, P.-F.; Azizi, M.; D'Escamard, V.; Di Narzo, A.F.; Kadian-Dodov, D.; Olin, J.W.; Kovacic, J.C.; Warchol-Celinska, E.; Prejbisz, A.; Januszewicz, A.; Baranowska, A.A.; Webb, T.R.; Hamby, S.E.; Samani, N.J.; Adlam, D.; Fendrikova-Mahlay, N.; Hazen, S.; Wang, Y.; Yang, M.-L.; Hunker, K.; Ganesh, S.K.; Combaret, N.; Motreff, P.; Azarine, A.; Gornik, H.L.
Source
In: Cardiovascular Research . (Cardiovascular Research, 1 April 2021, 117(4):1154-1165)
Subject
Language
English
ISSN
17553245
00086363
00086363