Vascular Ehlers-Danlos syndrome, an often unrecognized clinical entity: a case report of a novel mutation in the COL3A1 gene

por Huljev Frković, Sanda, Marija Slišković, Ana, Toivonen, Mia, Crkvenac Gregorek, Andrea, Šutalo, Ana, Vrkić Kirhmajer, Majda
Publicado 2022