Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Noon Mousa"'
Autor:
Fowzan S. Alkuraya, Shinu Ansari, Nadia Al-Hashmi, Eissa Faqeih, Anas M. Alazami, Noon Mousa, Aisha Alsinani, Zayed S. Al-Zayed, Fatema Alzahrani, Mohammed Al-Owain, Ranad Shaheen, Muneera J. Alshammari
Publikováno v:
Journal of Medical Genetics. 49:630-635
Background Osteogenesis imperfecta (OI) is an hereditary bone disease in which increased bone fragility leads to frequent fractures and other complications, usually in an autosomal dominant fashion. An expanding list of genes that encode proteins rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9dbef9bd39bde5734b932f9acd12496
https://doi.org/10.1136/jmedgenet-2012-101142
https://doi.org/10.1136/jmedgenet-2012-101142
