A Ciliary Protein EVC2/LIMBIN Plays a Critical Role in the Skull Base for Mid-Facial Development

Ellis-van Creveld (EvC) syndrome is an autosomal recessive chondrodysplastic disorder. Affected patients present a wide spectrum of symptoms including short stature, postaxial polydactyly, and dental abnormalities. We previously disrupted Evc2, one of the causative genes for EvC syndrome, in mice us...

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Detalles Bibliográficos
Autores principales: Kulkarni, Anshul K., Louie, Ke’ale W., Yatabe, Marilia, Ruellas, Antonio Carlos de Oliveira, Mochida, Yoshiyuki, Cevidanes, Lucia H. S., Mishina, Yuji, Zhang, Honghao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210651/
https://www.ncbi.nlm.nih.gov/pubmed/30410447
http://dx.doi.org/10.3389/fphys.2018.01484

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210651/
https://www.ncbi.nlm.nih.gov/pubmed/30410447
http://dx.doi.org/10.3389/fphys.2018.01484

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