Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I.

Abstract

Dentin dysplasia type I (DDI) is an autosomal-dominant genetic disorder resulting from dentin defects. The molecular basis of DDI remains unclear. DDI exhibits unique characteristics with phenotypes featuring obliteration of pulp chambers and diminutive root, thus providing a useful model for understanding the genetics of tooth formation. Using a large… (More)
DOI: 10.1002/humu.23130

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