A common SNP risk variant MT1-MMP causative for Dupuytren’s Disease has a specific defect in collagenolytic activity (Matrix Biology, 2021)

(untitled) - Itoh, Y; Ng, M; Wiberg, A; Inoue, K; Hirata, N; Paiva, K; Ito, N; Dzobo, K; Sato, N; Gifford, V; Fujita, Y; Inada, M; et al.