Enamel and dentin in Enamel renal syndrome: A confocal Raman microscopy view

Enamel Renal Syndrome (ERS) is a rare genetic disorder caused by biallelic mutations in Family with sequence similarity 20A (FAM20A) gene encoding the secretory pathway pseudokinase FAM20A. ERS is characterized by hypoplastic amelogenesis imperfecta (AI), impaired tooth eruption, intra-pulpal calcif...

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Detalles Bibliográficos
Autores principales: Desoutter, Alban, Cases, Olivier, Collart Dutilleul, Pierre Yves, Simancas Escorcia, Victor, Cannaya, Vidjea, Cuisinier, Frédéric, Kozyraki, Renata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453029/
https://www.ncbi.nlm.nih.gov/pubmed/36091358
http://dx.doi.org/10.3389/fphys.2022.957110

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453029/
https://www.ncbi.nlm.nih.gov/pubmed/36091358
http://dx.doi.org/10.3389/fphys.2022.957110

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