Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop’s classification

Amelogenesis imperfecta (AI) is a heterogeneous group of genetic rare diseases disrupting enamel development (Smith et al., Front Physiol, 2017a, 8, 333). The clinical enamel phenotypes can be described as hypoplastic, hypomineralized or hypomature and serve as a basis, together with the mode of inh...

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Detalles Bibliográficos
Autores principales: Bloch-Zupan, Agnes, Rey, Tristan, Jimenez-Armijo, Alexandra, Kawczynski, Marzena, Kharouf, Naji, Dure-Molla, Muriel de La, Noirrit, Emmanuelle, Hernandez, Magali, Joseph-Beaudin, Clara, Lopez, Serena, Tardieu, Corinne, Thivichon-Prince, Béatrice, Dostalova, Tatjana, Macek, Milan, Alloussi, Mustapha El, Qebibo, Leila, Morkmued, Supawich, Pungchanchaikul, Patimaporn, Orellana, Blanca Urzúa, Manière, Marie-Cécile, Gérard, Bénédicte, Bugueno, Isaac Maximiliano, Laugel-Haushalter, Virginie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205041/
https://www.ncbi.nlm.nih.gov/pubmed/37228816
http://dx.doi.org/10.3389/fphys.2023.1130175

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205041/
https://www.ncbi.nlm.nih.gov/pubmed/37228816
http://dx.doi.org/10.3389/fphys.2023.1130175

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