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Mutant DLX 3 disrupts odontoblast polarization and dentin formation
Tricho-dento-osseous (TDO) syndrome is an autosomal dominant disorder characterized by abnormalities in the thickness and density of bones and teeth. A 4-bp deletion mutation in the Distal-Less 3 (DLX3) gene is etiologic for most cases of TDO. To investigate the in vivo role of mutant DLX3 (MT-DLX3)...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2945701/ https://ncbi.nlm.nih.gov/pubmed/20510228 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ydbio.2010.05.499 |
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