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A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities
“Amelogenesis imperfecta” (AI) describes a group of genetic conditions that result in defects in tooth enamel formation. Mutations in many genes are known to cause AI, including the gene encoding the serine protease, kallikrein related peptidase 4 (KLK4), expressed during the maturation stage of ame...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447068/ https://www.ncbi.nlm.nih.gov/pubmed/28611678 http://dx.doi.org/10.3389/fphys.2017.00333 |