Hypomaturation Amelogenesis Imperfecta due to WDR72 Mutations: A Novel Mutation and Ultrastructural Analyses of Deciduous Teeth

BACKGROUND: Mutations in WDR72 have been identified in autosomal recessive hypomaturation amelogenesis imperfecta (AI). OBJECTIVE: to describe a novel WDR72 mutation and report the ultrastructural enamel phenotype associated with a different WDR72 mutation. METHODS: A family segregating autosomal re...

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Detalles Bibliográficos
Autores principales: El-Sayed, W., Shore, R.C., Parry, D.A., Inglehearn, C.F., Mighell, A.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2011
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128158/
https://www.ncbi.nlm.nih.gov/pubmed/21196691
http://dx.doi.org/10.1159/000322036

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128158/
https://www.ncbi.nlm.nih.gov/pubmed/21196691
http://dx.doi.org/10.1159/000322036

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