Rare loss-of-function mutations of <i>PTGIR</i> are enriched in fibromuscular dysplasia
Adrien Georges(Délégation Paris 7), Nabila Bouatia‐Naji(Inserm), B. Fiquet(Hôpital Européen Georges-Pompidou), Kristina L. Hunker(University of Michigan), Anna Baranowska(University of Leicester), Patrick Bruneval(Hôpital Européen), Ewa Warchoł-Celińska(Institute of Cardiology), Natalia Fendrikova-Mahlay(Cleveland Clinic), Stanley L. Hazen(Cleveland State University), Xavier Jeunemaı̂tre(Inserm), Stephen E. Hamby(University of Leicester), Andrzej Januszewicz(Institute of Cardiology), 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(Délégation Paris 5), 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 of Leicester), 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(Université Paris Cité), Antonio Di Narzo(Cardiovascular Institute of the South), Jason C. Kovacic(Cardiovascular Institute of the South), Yu Wang(Council of Independent Colleges), Pierre‐François Plouin(Hôpital Broussais), Délia Dupré(Inserm), Heather L. Gornik(University of Pittsburgh Medical Center), Pascal Motreff(Université Clermont Auvergne), Aurélien Lorthioir(Assistance Publique – Hôpitaux de Paris)
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