Theoretical representation explaining protein aggregation in stromal “spaces”. S. Kamma-LorgerChristina PinaliChristian Carlos MartínezJuan HarrisJon YoungRobert D. BredrupCecilie CrosasEva MalfoisMarc RødahlEyvind M. MeekKeith KnuppCarlo 2016 <p>The mutation in Decorin in the case of CSCD did not affect the protein’s ability to form dimers, but prevented it from interacting with collagen and caused it to subsequently aggregate in lamellar gaps in the diseased stroma. The aggregated molecules formed anti-parallel associations. The regions with the protein cores are unstained and invisible, whereas the two fold axes are where the red diamonds are.</p>