Detection of a rare AXIN2 variant in an Iranian family with hypodontia and oligodontia
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DOI: 10.34172/joddd.2022.018
Abstract: Background. Hypodontia, or the absence of one or more teeth during tooth formation, is a highly prevalent dental anomaly. Nevertheless, the main causes are still unknown. Mutations in PAX9, MSX1, WNT10A, and AXIN2 genes are… read more here.
Keywords: family; variant; iranian family; hypodontia oligodontia ... See more keywords