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Mutations in WNT1 are a cause of osteogenesis imperfecta

by: Somayyeh Fahiminiya, Jacek Majewski, John Mort, Pierre Moffatt, Francis H. Glorieux, Frank Rauch
Journal of Medical Genetics (23 February 2013), doi:10.1136/jmedgenet-2013-101567  Key: citeulike:12101688

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Abstract

Background Osteogenesis imperfecta (OI) is a heritable bone fragility disorder that is usually due to dominant mutations in COL1A1 or COL1A2. Rare recessive forms of OI, caused by mutations in genes involved in various aspects of bone formation, have been described as well.


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