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"Lessons from Rare Forms of Osteoarthritis".
Shepherd RF, Kerns JG, Ranganath LR, Gallagher JA, Taylor AM. Shepherd RF, et al. Calcif Tissue Int. 2021 Sep;109(3):291-302. doi: 10.1007/s00223-021-00896-3. Epub 2021 Aug 21. Calcif Tissue Int. 2021. PMID: 34417863 Free PMC article. Review.
In some of these rarer forms, single defective genes are responsible. The extreme phenotypes seen in conditions such as Camptodactyly Arthropathy-Coxa Vara-pericarditis Syndrome, Chondrodysplasias and Alkaptonuria all present potential op …
In some of these rarer forms, single defective genes are responsible. The extreme phenotypes seen in conditions such as Camptodactyly
Lubricin: a novel potential biotherapeutic approaches for the treatment of osteoarthritis.
Bao JP, Chen WP, Wu LD. Bao JP, et al. Mol Biol Rep. 2011 Jun;38(5):2879-85. doi: 10.1007/s11033-010-9949-9. Epub 2010 Jan 23. Mol Biol Rep. 2011. PMID: 20099082 Review.
Moreover, mutations or lacking of lubricin gene have been shown to link to the joint disease such as camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP), synovial hyperplasia and failure of joint function, suggesting an impor …
Moreover, mutations or lacking of lubricin gene have been shown to link to the joint disease such as camptodactyly-arthropathy