Severe osteogenesis imperfecta in cyclophilin B-deficient mice
Severe osteogenesis imperfecta in cyclophilin B-deficient mice
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United States: Public Library of Science
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Language
English
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Publisher
United States: Public Library of Science
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Contents
Osteogenesis Imperfecta (OI) is a human syndrome characterized by exquisitely fragile bones due to osteoporosis. The majority of autosomal dominant OI cases result from point or splice site mutations in the type I collagen genes, which are thought to lead to aberrant osteoid within developing bones. OI also occurs in humans with homozygous mutation...
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Full title
Severe osteogenesis imperfecta in cyclophilin B-deficient mice
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TN_cdi_plos_journals_1313571604
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1313571604
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ISSN
1553-7404,1553-7390
E-ISSN
1553-7404
DOI
10.1371/journal.pgen.1000750
