Phenotype and enamel ultrastructure characteristics in patients with ENAM gene mutations g.13185–13186insAG and 8344delG
Author:
Publisher
Elsevier BV
Subject
Cell Biology,General Dentistry,General Medicine,Otorhinolaryngology
Reference24 articles.
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2. The developing enamel matrix: nature and function;Robinson;Eur J Oral Sci,1998
3. A comparison of enamelin and amelogenin expression in developing mouse molars;Hu;Eur J Oral Sci,2001
4. Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta;Rajpar;Hum Mol Genet,2001
5. Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects;Hart;J Med Genet,2003
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3. Molecular‐based phenotype variations in amelogenesis imperfecta;Oral Diseases;2023-05-08
4. Novel ITGB6 variants cause hypoplastic-hypomineralized amelogenesis imperfecta and taurodontism: characterization of tooth phenotype and review of literature;BDJ Open;2023-04-11
5. A novel ENAM mutation causes hypoplastic amelogenesis imperfecta;Oral Diseases;2021-05-04
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