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pro vyhledávání: '"Joëlle Tanniger"'
Autor:
Alexandra Lenoir, Bérengère Aubry-Rozier, Aline Bregou, Elena Gonzalez Rodriguez, Célia Paquier, Joëlle Tanniger, Mohamed Faouzi, Romain Lazor
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-12 (2024)
Abstract Background Osteogenesis imperfecta (OI) is a rare hereditary bone disease resulting from a defect in collagen synthesis or processing, leading to bone fragility, frequent fractures and skeletal deformities. OI is associated with increased re
Externí odkaz:
https://doaj.org/article/263fa2d3bb654868a4d760d3845bc245
