Associated Papers
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
Novel FAM83H mutations in patients with amelogenesis imperfecta.
Xin W et al.
Scientific Reports, 2017
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