A novel <it>DSPP </it>mutation causes dentinogenesis imperfecta type II in a large Mongolian family
<p>Abstract</p> <p>Background</p> <p>Several studies have shown that the clinical phenotypes of dentinogenesis imperfecta type II (DGI-II) may be caused by mutations in <it>dentin sialophosphoprotein </it>(<it>DSPP</it>). However, no previous stu...
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BMC,
2010-02-01T00:00:00Z.
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