Associated Papers
AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta.
Wang SK et al.
International Journal of Molecular Sciences, 2024
38892321 (PubMed )
Supplement: ijms-25-06132-s001.zip › ijms-3003435-supplementary.pdf
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
Leban T et al.
Genes, 2022
A Novel AMELX Mutation, Its Phenotypic Features, and Skewed X Inactivation.
Duan X et al.
Journal of Dental Research, 2019
Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry.
Urzúa B et al.
Biochemical Genetics, 2011
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