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The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V

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author: Gareth Baynam  Gethin Thomas  Emma L. Duncan  Craig F. Munns  Aideen M McInerney-Leo  Matthew A. Brown 

Publication date March 27, 2014
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