Mobility in Osteogenesis Imperfecta: A Multicenter North American Study

BACKGROUND: Osteogenesis imperfecta (OI) is a genetic connective tissue disorder characterized by increased bone fragility and recurrent fractures. The phenotypic severity of OI has a significant influence on the ability to walk but little is known about the ambulatory characteristics, strength, or...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Genet Med
Päätekijät: Kruger, Karen M., Caudill, Angela, Celin, Mercedes Rodriguez, Nagamani, Sandesh CS, Shapiro, Jay R, Steiner, Robert D, Bober, Michael B, Hart, Tracy, Cuthbertson, David, Krischer, Jeff, Byers, Peter H, Durigova, Michaela, Glorieux, Francis H, Rauch, Frank, Sutton, V Reid, Lee, Brendan, Rush, Eric T, Smith, Peter A., Harris, Gerald F.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2019
Aiheet:
Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7401984/
https://ncbi.nlm.nih.gov/pubmed/30918359
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41436-019-0491-4
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