Biomechanical properties of bone in a mouse model of Rett syndrome

Rett syndrome (RTT) is an X-linked genetic disorder and a major cause of intellectual disability in girls. Mutations in the methyl-CpG binding protein 2 (MECP2) gene are the primary cause of the disorder. Despite the dominant neurological phenotypes, MECP2 is expressed ubiquitously throughout the bo...

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Detalles Bibliográficos
Autores principales: Kamal, Bushra, Russell, David, Payne, Anthony, Constante, Diogo, Tanner, K. Elizabeth, Isaksson, Hanna, Mathavan, Neashan, Cobb, Stuart R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2015
Materias:
Original Full Length Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289916/
https://www.ncbi.nlm.nih.gov/pubmed/25445449
http://dx.doi.org/10.1016/j.bone.2014.10.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289916/
https://www.ncbi.nlm.nih.gov/pubmed/25445449
http://dx.doi.org/10.1016/j.bone.2014.10.008

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