Mutations in <it>FKBP10 </it>can cause a severe form of isolated Osteogenesis imperfecta

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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Bibliographic Details
Main Authors: Steinlein Ortrud K, Aichinger Eric, Trucks Holger, Sander Thomas
Format: Article
Language:English
Published: BMC 2011-11-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/12/152

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