Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1)
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference25 articles.
1. Genetic heterogeneity in X-linked amelogenesis imperfecta
2. Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)
3. Permanent tooth sizes in 46, XX-males
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1. Mutations Causing X-Linked Amelogenesis Imperfecta Alter miRNA Formation from Amelogenin Exon4;Journal of Dental Research;2023-08-10
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3. Calcium interactions in amelogenin-derived peptide assembly;Frontiers in Physiology;2022-12-14
4. An Intron c.103-3T>C Variant of the AMELX Gene Causes Combined Hypomineralized and Hypoplastic Type of Amelogenesis Imperfecta: Case Series and Review of the Literature;Genes;2022-07-18
5. Full Mouth Rehabilitation Using the Twin Stage Procedure in a Patient with Amelogenesis Imperfecta: A Case Report;Cureus;2022-05-31
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