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Altered Enamelin Phosphorylation Site Causes Amelogenesis Imperfecta

Defects in the enamelin gene (ENAM) cause amelogenesis imperfecta (AI). Our objective was to identify the genetic etiology of enamel hypoplasia in a Caucasian proband. Our hypothesis was that ENAM was defective. The proband and his father have an AG insertion (g.13185_13186insAG; p.422FsX448) in ENA...

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Detalhes bibliográficos
Main Authors: Chan, H.-C., Mai, L., Oikonomopoulou, A., Chan, H.L., Richardson, A.S., Wang, S.-K., Simmer, J.P., Hu, J.C.-C.
Formato: Artigo
Idioma:Inglês
Publicado em: SAGE Publications 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2889023/
https://ncbi.nlm.nih.gov/pubmed/20439930
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034510365662
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