Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen
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| Description | scientific article published on 4 September 2012 |
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author: Gerard Pals Arunkanth Ankala Kwame Anyane-Yeboa Louanne Hudgins Peter H. Byers Julia Wynn Robert D. Steiner |
| Publication date | September 4, 2012 |
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