Article
Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families.
Molecular genetics & genomic medicine - 1 May 2018
Taleb Kawther, Lauridsen Eva, Daugaard-Jensen Jette, Nieminen Pekka, Kreiborg Sven
Abstract excerpt
BACKGROUND: Dentinogenesis imperfecta (DI) is a rare debilitating hereditary disorder affecting dentin formation and causing loss of the overlying enamel. Clinically, DI sufferers have a discolored and weakened dentition with an increased risk of fracture. The aims of this study were to assess genotype-phenotype findings in three families with DI-II with special reference to mutations in the DSPP gene and...
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