DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference20 articles.
1. Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)
2. The Dlx3 protein harbors basic residues required for nuclear localization, transcriptional activity and binding to Msx1
3. Enamelin maps to human chromosome 4q21 within the autosomal dominant amelogenesis imperfecta locus
4. Transcriptional activation by the homeodomain protein Distal-less 3
5. Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q
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