Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen

U. Schwarze, T. Cundy, S.M. Pyott, H.E. Christiansen, M.R. Hegde, R.A. Bank, G. Pals, A. Ankala, K. Conneely, L. Seaver, S.M. Yandow, E. Raney, D. Babovic-Vuksanovic, J. Stoler, Z. Ben-Neriah, R. Segel, S. Lieberman, L. Siderius, A. Al-Aqeel, M. HannibalL. Hudgins, E. McPherson, M. Clemens, M.D. Sussman, R.D. Steiner, J. Mahan, R. Smith, K. Anyane-Yeboa, J. Wynn, K. Chong, T. Uster, S. Aftimos, V.R. Sutton, E.C. Davis, L.S. Kim, M.A. Weis, D. Eyre, P.H. Byers

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)1-17
JournalHuman Molecular Genetics
Volume22
Issue number1
DOIs
Publication statusPublished - 2013

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