FAM20A Gene Mutation: Amelogenesis or Ectopic Mineralization?

Background and objective: FAM20A gene mutations result in enamel renal syndrome (ERS) associated with amelogenesis imperfecta (AI), nephrocalcinosis, gingival fibromatosis, and impaired tooth eruption. FAM20A would control the phosphorylation of enamel peptides and thus enamel mineralization. Here,...

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Detalles Bibliográficos
Autores principales: Lignon, Guilhem, Beres, Fleur, Quentric, Mickael, Rouzière, Stephan, Weil, Raphael, De La Dure-Molla, Muriel, Naveau, Adrien, Kozyraki, Renata, Dessombz, Arnaud, Berdal, Ariane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413562/
https://www.ncbi.nlm.nih.gov/pubmed/28515694
http://dx.doi.org/10.3389/fphys.2017.00267

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413562/
https://www.ncbi.nlm.nih.gov/pubmed/28515694
http://dx.doi.org/10.3389/fphys.2017.00267

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