Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature
Author:
Publisher
Elsevier BV
Subject
Cell Biology,General Dentistry,General Medicine,Otorhinolaryngology
Reference27 articles.
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1. Association between malocclusions and amelogenesis imperfecta genotype and phenotype: A systematic review;International Orthodontics;2023-12
2. Splicing mutations in AMELX and ENAM cause amelogenesis imperfecta;BMC Oral Health;2023-11-20
3. Molecular‐based phenotype variations in amelogenesis imperfecta;Oral Diseases;2023-05-08
4. A novel ENAM mutation causes hypoplastic amelogenesis imperfecta;Oral Diseases;2021-05-04
5. ENAM mutations and digenic inheritance;Molecular Genetics & Genomic Medicine;2019-09-02
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