Note: This list contains duplicate records, as identified by the OpenAIRE deduplication algorithm based on metadata analysis.
Severe cases of osteogenesis imperfecta type VIII due to a homozygous mutation in P3H1 (LEPRE1) and review of the literature
Advances in Clinical and Experimental Medicine · 2021 · 10.17219/acem/141367
Severe cases of osteogenesis imperfecta type VIII due to a homozygous mutation in P3H1 (LEPRE1) and review of the literature
Advances in Clinical and Experimental Medicine · 2021 · 34637196