Osteogenesis imperfecta
Author:
Funder
Fondazione Cariplo
Telethon
Publisher
Elsevier BV
Subject
General Medicine
Reference140 articles.
1. CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta;Morello;Cell,2006
2. Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta;Barnes;N Engl J Med,2006
3. New perspectives on osteogenesis imperfecta;Forlino;Nat Rev Endocrinol,2011
4. Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans;Marini;Hum Mutat,2007
5. New genes in bone development: what's new in osteogenesis imperfecta;Marini;J Clin Endocrinol Metab,2013
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