Mutations in <it>FKBP10 </it>can cause a severe form of isolated Osteogenesis imperfecta
<p>Abstract</p> <p>Background</p> <p>Mutations in the <it>FKBP10 </it>gene were first described in patients with Osteogenesis imperfecta type III. Two follow up reports found <it>FKBP10 </it>mutations to be associated with Bruck syndrome type 1,...
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| Main Authors: | , , , |
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| Format: | Book |
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BMC,
2011-11-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |