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IRF6 and SPRY4 Signaling Interact in Periderm Development
Rare mutations in IRF6 and GRHL3 cause Van der Woude syndrome, an autosomal dominant orofacial clefting disorder. Common variants in IRF6 and GRHL3 also contribute risk for isolated orofacial clefting. Similarly, variants within genes that encode receptor tyrosine kinase (RTK) signaling components,...
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| I publikationen: | J Dent Res |
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| Huvudupphovsmän: | , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
SAGE Publications
2017
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5613880/ https://ncbi.nlm.nih.gov/pubmed/28732181 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034517719870 |
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