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Autor:
Zhytnik, Lidiia, Maasalu, Katre, Duy, Ho Binh, Pashenko, Andrey, Khmyzov, Sergey, Reimann, Ene, Prans, Ele, Kõks, Sulev, Märtson, Aare
Background: Osteogenesis imperfecta (OI) is a rare genetic bone fragility disorder. In the current study, differences between the genotypes and phenotypes of de novo and inherited collagen‐related OI were investigated. Methods: A comparative analys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1018::46ac09415a77ddbb5996803899ab6b3a
http://hdl.handle.net/10062/72141
http://hdl.handle.net/10062/72141
