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pro vyhledávání: '"Allan James Richards"'
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-4 (2018)
Abstract Background Osteogenesis imperfecta (OI) is a rare primarily autosomal dominant condition in which the connective tissues of bones, ligaments and sclerae do not form properly. Typically, mutations in COL1A1 and COL1A2 genes lead to the defect
Externí odkaz:
https://doaj.org/article/6ae0d17a829840aea783f582d4450250