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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Bibliografske podrobnosti
izdano v:J Dent Res
Main Authors: Paul, B.J., Palmer, K., Sharp, J.C., Pratt, C.H., Murray, S.A., Dunnwald, M.
Format: Artigo
Jezik:Inglês
Izdano: SAGE Publications 2017
Teme:
Research Reports
Online dostop: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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