Whole-exome sequencing 677 aneurysm patients identifies multiple rare variants in the proprotein convertase FURIN causing impaired TGFB family signaling

Zongsheng He,Rosan L. Lechner,Arne Ijpma,Daphne Heijsman,Hence J. M. Verhagen,Sander ten Raa, Hennie T. Bruggewirth,Robert M. W. Hofstra,Danny F. E. Huylenbroeck,John W. M. Creemers,Danielle F. Majoor-Krakauer

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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