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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235620/
https://www.ncbi.nlm.nih.gov/pubmed/32455153
http://dx.doi.org/10.1016/j.bonr.2020.100281

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235620/
https://www.ncbi.nlm.nih.gov/pubmed/32455153
http://dx.doi.org/10.1016/j.bonr.2020.100281

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