Mutant fibrillin-1 monomers lacking EGF-like domains disrupt microfibril assembly and cause severe marfan syndrome

Liu, W.; Qian, C.; Comeau, K.; Brenn, T.; Furthmayr, H.; Francke, U.

Human Molecular Genetics 5(10): 1581-1587

1996

0964-6906

10.1093/hmg/5.10.1581

https://eurekamag.com/research/009/066/009066382.php