Itoh, Yoshifumi 
; Ng, Michael ; Wiberg, Akira ; Inoue, Katsuaki ; Hirata, Narumi ; Paiva, Katiucia Batista da Silva ; Ito, Noriko ; Dzobo, Kim ; Sato, Nanami ; Gifford, Valentina ; Fujita, Yasuyuki ; Inada, Masaki ; Furniss, Dominic
Fonte: Matrix Biology. Unidade: ICB
Assuntos: ANATOMIA, COLÁGENO, SISTEMA MUSCULOSQUELÉTICO, DOENÇAS MUSCULARES, FÁSCIA, HOMEOSTASE, FENÓTIPOS
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ITOH, Yoshifumi et al. A common SNP risk variant MT1-MMP causative for Dupuytren's disease has a specific defect in collagenolytic activity. Matrix Biology, p. 20 , 2021Tradução . . Disponível em: https://doi.org/10.1016/j.matbio.2021.02.003. Acesso em: 28 jun. 2024.APA
Itoh, Y., Ng, M., Wiberg, A., Inoue, K., Hirata, N., Paiva, K. B. da S., et al. (2021). A common SNP risk variant MT1-MMP causative for Dupuytren's disease has a specific defect in collagenolytic activity. Matrix Biology, 20 . doi:10.1016/j.matbio.2021.02.003NLM
Itoh Y, Ng M, Wiberg A, Inoue K, Hirata N, Paiva KB da S, Ito N, Dzobo K, Sato N, Gifford V, Fujita Y, Inada M, Furniss D. A common SNP risk variant MT1-MMP causative for Dupuytren's disease has a specific defect in collagenolytic activity [Internet]. Matrix Biology. 2021 ;20 .[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.matbio.2021.02.003Vancouver
Itoh Y, Ng M, Wiberg A, Inoue K, Hirata N, Paiva KB da S, Ito N, Dzobo K, Sato N, Gifford V, Fujita Y, Inada M, Furniss D. A common SNP risk variant MT1-MMP causative for Dupuytren's disease has a specific defect in collagenolytic activity [Internet]. Matrix Biology. 2021 ;20 .[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.matbio.2021.02.003
