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Article

Dental and facial characteristics of osteogenesis imperfecta type V

2018-09-11

Abstract excerpt

Osteogenesis imperfecta (OI) type V is an ultrarare heritable bone disorder caused by the heterozygous c.-14C>T mutation in IFITM5 . The dental and craniofacial phenotype has not been described in detail. In the present multicenter study (Brittle Bone Disease Consortium) 14 individuals with OI type V (age 3 to 50 years; 10 females, 4 males) underwent dental and craniofacial assessment. None of the individuals had...

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Literature Corpus work
bd36bbc2-ea1e-53d0-b1e6-b4559ccc6caa
DOI
10.1101/413633
Open publication

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Dental and facial characteristics of osteogenesis imperfecta type VDOI 10.1101/413633
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