Article
An SNP variant MT1-MMP with a defect in its collagenolytic activity confers the fibrotic…
medRxiv · 2020 · Itoh, Y.; Ng, M.; Wiberg, A.; Inoue, K.; Hirata, N.; Paiva, K. B.; Ito, N.; Dzobo, K.; Sato, N.; Gifford, V.; Fijita, Y.; Inada, M.; Furniss, D.
Key facts
| Title | An SNP variant MT1-MMP with a defect in its collagenolytic activity confers the fibrotic phenotype of Dupuytren’s Disease |
|---|---|
| First author | Itoh, Y.; Ng, M.; Wiberg, A.; Inoue, K.; Hirata, N.; Paiva, K. B.; Ito, N.; Dzobo, K.; Sato, N.; Gifford, V.; Fijita, Y.; Inada, M.; Furniss, D. |
| Journal | medRxiv |
| Published | Jun 12, 2020 |
| DOI | 10.1101/2020.06.09.142513 |
| Product codes mentioned | JCJ, KIP, KIT, NDS, NJT |
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- None FDA submissions mentioned
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