A novel <it>DSPP </it>mutation is associated with type II dentinogenesis Imperfecta in a chinese family

• Главные авторы: Xu Chengqi (Автор), Wang Xiaotao (Автор), Chang Wei (Автор), Zhao Zhen (Автор), Qu Erjun (Автор), Chen Lanying (Автор), Liu Jingyu (Автор), Zhang Xianqin (Автор), Wang Qing K (Автор), Liu Mugen (Автор)
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• Опубликовано: BMC, 2007-08-01T00:00:00Z.
• Предметы: article
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<p>Abstract</p> <p>Background</p> <p>Hereditary defects of tooth dentin are classified into two main groups: dentin dysplasia (DD) (types I and II) and dentinogenesis imperfecta (DGI) (types I, II, and III). Type II DGI is one of the most common tooth defects with an au...