Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen (Q36709687)
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scientific article published on 4 September 2012
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen |
scientific article published on 4 September 2012 |
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Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen (English)
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Julia Wynn
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Louanne Hudgins
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Ulrike Schwarze
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Tim Cundy
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Shawna M Pyott
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Helena E Christiansen
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Madhuri R Hegde
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Ruud A Bank
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Karen Conneely
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Laurie Seaver
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Suzanne M Yandow
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Ellen Raney
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Dusica Babovic-Vuksanovic
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Joan Stoler
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Ziva Ben-Neriah
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Reeval Segel
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Sari Lieberman
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Liesbeth Siderius
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Aida Al-Aqeel
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Mark Hannibal
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Elizabeth McPherson
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Michele Clemens
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Michael D Sussman
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John Mahan
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Rosemarie Smith
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Karen Chong
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Tami Uster
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Salim Aftimos
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V Reid Sutton
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Elaine C Davis
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Lammy S Kim
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Mary Ann Weis
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David Eyre
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Identifiers
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