Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta
<p>Abstract</p> <p>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 evidenc...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2007-01-01
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| Series: | Head & Face Medicine |
| Online Access: | http://www.head-face-med.com/content/3/1/8 |