IndraLab

Statements


SCN8A activates mutated COMP. 1 / 1
| 1

reach
"This finding is especially important given the role of type XIV in collagen fibrillogenesis, the known disruption to collagen fibrillogenesis caused by an MED causing COMP mutation and the previous finding of altered collagen fibril morphology in Matn3 V194D, Comp DelD469 and Comp T585M cartilages (supplementary material Fig."