Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function

Ciliopathies are a group of genetic disorders caused by defective assembly or dysfunction of the primary cilium, a microtubule-based cellular organelle that plays a key role in developmental signalling. Ciliopathies are clinically grouped in a large number of overlapping disorders, including the oro...

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Detalles Bibliográficos
Autores principales: Cortés, Claudio R., McInerney-Leo, Aideen M., Vogel, Ida, Rondón Galeano, Maria C., Leo, Paul J., Harris, Jessica E., Anderson, Lisa K., Keith, Patricia A., Brown, Matthew A., Ramsing, Mette, Duncan, Emma L., Zankl, Andreas, Wicking, Carol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837335/
https://www.ncbi.nlm.nih.gov/pubmed/27094867
http://dx.doi.org/10.1038/srep24083

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837335/
https://www.ncbi.nlm.nih.gov/pubmed/27094867
http://dx.doi.org/10.1038/srep24083

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