Gawron K

ORCID: 0000-0003-3430-6270 · 1 paper in corpus
2023
Analysis of miRNAs in Osteogenesis imperfecta Caused by Mutations in COL1A1 and COL1A2: Insights into Molecular Mechanisms and Potential Therapeutic Targets.
Pharmaceuticals (Basel, Switzerland) ·doi:10.3390/ph16101414

Osteogenesis imperfecta (OI) is a group of connective tissue disorders leading to abnormal bone formation, mainly due to mutations in genes encoding collagen type I (Col I). Osteogenesis is regulated by a number of molecules, including micr…