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Elsevier, Matrix Biology, (97), p. 20-39, 2021

DOI: 10.1016/j.matbio.2021.02.003

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A common SNP risk variant MT1-MMP causative for Dupuytren's Disease has a specific defect in collagenolytic activity

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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