Osteogenesis Imperfecta, an Ever-Expanding Conundrum
Author:
Affiliation:
1. Shriners Hospital for Children and McGill University; Montreal, QC Canada
Publisher
Wiley
Subject
Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jbmr.1982/fullpdf
Reference46 articles.
1. Osteogenesis Imperfecta
2. Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease;Ward;Bone.,2002
3. CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta;Morello;Cell.,2006
4. New perspectives on osteogenesis imperfecta;Forlino;Nat Rev Endocrinol.,2011
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