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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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Udgivet i: | Front Physiol |
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Main Authors: | , , , , , , , |
Format: | Artigo |
Sprog: | Inglês |
Udgivet: |
Frontiers Media S.A.
2018
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Fag: | |
Online adgang: | 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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