Osteogenesis imperfecta (OI) is an inherited (genetic) bone disorder that is present at birth. It is also known as brittle ...
When Columbus resident Jennifer Roberts’ family gets together for the holidays, they typically play a few games of bingo for ...
Osteogenesis imperfecta (OI), also known as brittle bone disease, is a rare genetic disease affecting the connective tissue and bones. In this disease, bones become extremely fragile and break or ...
You have full access to this article via your institution. In human JEB, besides mutations of the laminin-5 gene, mutations in type XVII collagen and α6β4-integrin genes have been reported 25.
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