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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Bibliografiset tiedot
Julkaisussa:Front Physiol
Päätekijät: Kulkarni, Anshul K., Louie, Ke’ale W., Yatabe, Marilia, Ruellas, Antonio Carlos de Oliveira, Mochida, Yoshiyuki, Cevidanes, Lucia H. S., Mishina, Yuji, Zhang, Honghao
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2018
Aiheet:
Physiology
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6210651/
https://ncbi.nlm.nih.gov/pubmed/30410447
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2018.01484
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