Osteogenesis imperfecta type 3 in South Africa: Causative mutations in FKBP10

Volume: 107, Issue: 5, Pages: 457 - 457
Published: Apr 25, 2017
Abstract
Background. A relatively high frequency of autosomal recessively inherited osteogenesis imperfecta (OI) type 3 (OI-3) is present in the indigenous black southern African population. Affected persons may be severely handicapped as a result of frequent fractures, progressive deformity of the tubular bones and spinal malalignment. Objective. To delineate the molecular basis for the condition. Methods. Molecular investigations were performed on 91...
Paper Details
Title
Osteogenesis imperfecta type 3 in South Africa: Causative mutations in FKBP10
Published Date
Apr 25, 2017
Volume
107
Issue
5
Pages
457 - 457
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