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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Detalles Bibliográficos
Autores principales: Coxon, Thomas Liam, Brook, Alan Henry, Barron, Martin John, Smith, Richard Nigel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2012
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718574/
https://www.ncbi.nlm.nih.gov/pubmed/22759786
http://dx.doi.org/10.1159/000336440

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718574/
https://www.ncbi.nlm.nih.gov/pubmed/22759786
http://dx.doi.org/10.1159/000336440

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