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Phenotype-Genotype Correlations in Mouse Models of Amelogenesis Imperfecta Caused by Amelx and Enam Mutations

Mutations in human and in mouse orthologous genes Amelx and Enam result in a diverse range of enamel defects. In this study we aimed to investigate the phenotype-genotype correlation between the mutants and the wild-type controls in mouse models of amelogenesis imperfecta using novel measurement app...

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Détails bibliographiques
Auteurs principaux: Coxon, Thomas Liam, Brook, Alan Henry, Barron, Martin John, Smith, Richard Nigel
Format: Artigo
Langue:Inglês
Publié: S. Karger AG 2012
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3718574/
https://ncbi.nlm.nih.gov/pubmed/22759786
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000336440
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