Results
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4821.
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4822.
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4823.
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4824.
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4825.
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4826.
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4827.
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4828.
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4829.
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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. [electronic resource] by
- Schwarze, Ulrike
- Cundy, Tim
- Pyott, Shawna M
- Christiansen, Helena E
- Hegde, Madhuri R
- Bank, Ruud A
- Pals, Gerard
- Ankala, Arunkanth
- Conneely, Karen
- Seaver, Laurie
- Yandow, Suzanne M
- Raney, Ellen
- Babovic-Vuksanovic, Dusica
- Stoler, Joan
- Ben-Neriah, Ziva
- Segel, Reeval
- Lieberman, Sari
- Siderius, Liesbeth
- Al-Aqeel, Aida
- Hannibal, Mark
- Hudgins, Louanne
- McPherson, Elizabeth
- Clemens, Michele
- Sussman, Michael D
- Steiner, Robert D
- Mahan, John
- Smith, Rosemarie
- Anyane-Yeboa, Kwame
- Wynn, Julia
- Chong, Karen
- Uster, Tami
- Aftimos, Salim
- Sutton, V Reid
- Davis, Elaine C
- Kim, Lammy S
- Weis, Mary Ann
- Eyre, David
- Byers, Peter H
Producer: 20130515
In:
Human molecular genetics vol. 22
Availability: No items available.
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4830.
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4831.
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4832.
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4833.
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4834.
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4835.
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4836.
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4837.
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4838.
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4839.
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4840.
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