Enamel Formation and Amelogenesis Imperfecta
Author:
Publisher
S. Karger AG
Subject
Histology,Anatomy
Reference76 articles.
1. Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)
2. Analysis of the LAMB3 gene in a junctional epidermolysis bullosa patient reveals exonic splicing and allele-specific nonsense-mediated mRNA decay
3. Enamelysin (Matrix Metalloproteinase 20)-deficient Mice Display an Amelogenesis Imperfecta Phenotype
4. The caries resistance of human teeth is determined by the spatial arrangement of hydroxyapatite microcrystals in the enamel
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