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ARHGAP29 Mutation Is Associated with Abnormal Oral Epithelial Adhesions
Nonsyndromic cleft lip and/or palate (NSCL/P) is a prevalent birth defect of complex etiology. Previous studies identified mutations in ARHGAP29 associated with an increased risk for NSCL/P. To investigate the effects of ARHGAP29 in vivo, we generated a novel murine allele by inserting a point mutat...
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| Publicado en: | J Dent Res |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
SAGE Publications
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5613885/ https://ncbi.nlm.nih.gov/pubmed/28817352 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034517726079 |
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