An amelogenin gene defect associated with human X-linked amelogenesis imperfecta
Author:
Publisher
Elsevier BV
Subject
Cell Biology,General Dentistry,General Medicine,Otorhinolaryngology
Reference26 articles.
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2. AMELX Mutations and Genotype–Phenotype Correlation in X-Linked Amelogenesis Imperfecta;International Journal of Molecular Sciences;2024-06-01
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