Rare loss-of-function mutations of <i>PTGIR</i> are enriched in fibromuscular dysplasia
Adrien Georges(Inserm), Nabila Bouatia‐Naji(Délégation Paris 5), B. Fiquet(Hôpital Européen Georges-Pompidou), Kristina L. Hunker(Michigan Medicine), Anna Baranowska(University of Leicester), Patrick Bruneval(Hôpital Européen), Ewa Warchoł-Celińska(Institute of Cardiology), Natalia Fendrikova-Mahlay(Cleveland Clinic), Stanley L. Hazen(Cleveland Clinic), Xavier Jeunemaı̂tre(Délégation Paris 5), Stephen E. Hamby(University of Leicester), Andrzej Januszewicz(Hypertension Institute), Daniella Kadian‐Dodov(Cardiovascular Institute of the South), Min‐Lee Yang(University of Michigan), Élie Mousseaux(MACOM (United States)), Jeffrey W. Olin(Icahn School of Medicine at Mount Sinai), Michel Azizi(Inserm), Santhi K. Ganesh(University of Michigan), Valentina d’Escamard(Icahn School of Medicine at Mount Sinai), Arshid Azarine(Hôpital Européen Georges-Pompidou), Aleksander Prejbisz(Institute of Cardiology), David Adlam(University College London), Laurence Amar(Unit of Functional and Adaptive Biology), Tom R. Webb(NIHR Leicester Biomedical Research Centre), Antoine Chédid(Hôpital Européen Georges-Pompidou), Nicolas Combaret(Centre National de la Recherche Scientifique), Takiy-Eddine Berrandou(Inserm), Juliette Albuisson(Délégation Paris 5), Antonio Di Narzo(Cardiovascular Institute of the South), Jason C. Kovacic(Victor Chang Cardiac Research Institute), Yu Wang(Council of Independent Colleges), Pierre‐François Plouin(Hôpital Broussais), Délia Dupré(Inserm), Heather L. Gornik(Asia Society), Pascal Motreff(Université Clermont Auvergne), Aurélien Lorthioir(Assistance Publique – Hôpitaux de Paris)
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