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Any osteogenesis imperfecta in which the cause of the disease is a variant in the COL1A2 gene.
No clinical trials have been registered for COL1A2-related osteogenesis imperfecta.
5 publications have been identified in PubMed for COL1A2-related osteogenesis imperfecta. Research spans Case Report / Case Series (40%), Epidemiology / Natural History (40%), and Review / Meta-Analysis (20%).
Blaschitz A (2026). [PMID: 41985044](https://pubmed.ncbi.nlm.nih.gov/41985044/). *Eur J Endocrinol*. [Case Report / Case Series]
Patiño-Salazar JD (2025). [PMID: 39915337](https://pubmed.ncbi.nlm.nih.gov/39915337/). *Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA*. [Epidemiology / Natural History]
Hassib NF (2025). [PMID: 40602110](https://pubmed.ncbi.nlm.nih.gov/40602110/). *Archives of oral biology*. [Review / Meta-Analysis]
Byrwa-Sztaba A (2025). [PMID: 40649786](https://pubmed.ncbi.nlm.nih.gov/40649786/). *International journal of molecular sciences*. [Epidemiology / Natural History]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 8:41 AM UTC
Common questions about COL1A2-related osteogenesis imperfecta