Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta
Author:
Publisher
Elsevier BV
Subject
Cell Biology,General Dentistry,General Medicine,Otorhinolaryngology
Reference21 articles.
1. Heritable defects of enamel;Witkop,1976
2. Amelogenesis imperfecta: prevalence and incidence in northern Swedish county;Backman;Community Dent Oral Epidemiol,1986
3. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification;Witkop;J Oral Pathol,1989
4. A deletion in the amelogenin gene in a family with X-linked amelogenesis imperfecta;Langerstrom;Genomics,1991
5. Genetic heterogeneity in X-linked amelogenesis imperfecta;Aldred;Genomics,1992
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2. Exploring the Pool of Pathogenic Variants of Amelogenesis Imperfecta: An Approach to the Understanding of Its Genetic Architecture;Frontiers in Dental Medicine;2021-11-26
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4. Control of Calcium Phosphate Nucleation and Transformation through Interactions of Enamelin and Amelogenin Exhibits the “Goldilocks Effect”;Crystal Growth & Design;2018-10-22
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