Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant.
Ulrike LepperdingerElisabeth MaurerMartina Witsch-BaumgartnerRobert StiglerJohannes ZschockeAdrian LussiInes Kapferer-SeebacherPublished in: Clinical oral investigations (2020)
The present report is expanding the clinical phenotype of SLC24A4 variants to more severe forms of amelogenesis imperfecta. An autosomal-dominant inheritance pattern with mild clinical phenotypes in heterozygotes has to be considered.
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