Deletion of amelotin exons 3–6 is associated with amelogenesis imperfecta

Amelogenesis imperfecta (AI) is a heterogeneous group of genetic conditions that result in defective dental enamel formation. Amelotin (AMTN) is a secreted protein thought to act as a promoter of matrix mineralization in the final stage of enamel development, and is strongly expressed, almost exclus...

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Detalles Bibliográficos
Autores principales: Smith, Claire E.L., Murillo, Gina, Brookes, Steven J., Poulter, James A., Silva, Sandra, Kirkham, Jennifer, Inglehearn, Chris F., Mighell, Alan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179951/
https://www.ncbi.nlm.nih.gov/pubmed/27412008
http://dx.doi.org/10.1093/hmg/ddw203

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179951/
https://www.ncbi.nlm.nih.gov/pubmed/27412008
http://dx.doi.org/10.1093/hmg/ddw203

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