Altered TGFΒ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type i caused by fibulin-4 deficiency

Marjolijn Renard, Tammy Holm, Regan Veith, Bert L. Callewaert, Lesley C. Adès, Osman Baspinar, Angela Pickart, Majed Dasouki, Juliane Hoyer, Anita Rauch, Pamela Trapane, Michael G. Earing, Paul J. Coucke, Lynn Y. Sakai, Harry C. Dietz, Anne M. De Paepe, Bart L. Loeys

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Medicine & Life Sciences