Osteogenesis Imperfecta Proteomic Characterisation Extracellular Vesicles
Osteogenesis Imperfecta (OI), known as ‘brittle bone disease’, is a rare heritable debilitating connective tissue disease, with incidence of approximately 1 in 20,000 birth. Majority of the cases are autosomal dominant in inheritance occurring due to mutations in genes encoding the α-chains α1 and α2...
