Gnathodiaphyseal dysplasia is not recapitulated in a respective mouse model carrying a mutation of the Ano5 gene

Mutations in the gene ANO5, encoding for the transmembrane protein Anoctamin 5 (Ano5), have been identified to cause gnathodiaphyseal dysplasia (GDD) in humans, a skeletal disorder characterized by sclerosis of tubular bones, increased fracture risk and fibro-osseous lesions of the jawbones. To bett...

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Detalhes bibliográficos
Publicado no:Bone Rep
Main Authors: Rolvien, Tim, Avci, Osman, von Kroge, Simon, Koehne, Till, Selbert, Stefan, Sonntag, Stephan, Shmerling, Doron, Kornak, Uwe, Oheim, Ralf, Amling, Michael, Schinke, Thorsten, Yorgan, Timur Alexander
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7235620/
https://ncbi.nlm.nih.gov/pubmed/32455153
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bonr.2020.100281
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