Phenotypic Variability in LAMA3-Associated Amelogenesis Imperfecta.
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DOI: 10.1111/odi.14425
Abstract: OBJECTIVE Amelogenesis imperfecta (AI) is defined as inherited enamel malformations. LAMA3 (laminin alpha-3) encodes a critical protein component of the basement membrane (laminin-332). Individuals carrying heterozygous LAMA3 mutations have previously been shown to have localized… read more here.
Keywords: lama3 mutations; amelogenesis imperfecta; enamel; enamel defects ... See more keywords