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Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta
Amelogenesis imperfecta (AI) is a genetically heterogeneous group of diseases that result in defective development of tooth enamel. Mutations in several enamel proteins and proteinases have been associated with AI. The object of this study was to evaluate evidence of etiology for the six major candi...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1800839/ https://ncbi.nlm.nih.gov/pubmed/17266769 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1746-160X-3-8 |
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