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
Dive into the research topics of 'Altered TGFΒ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type i caused by fibulin-4 deficiency'. Together they form a unique fingerprint.