Article
De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family.
European journal of oral sciences - 1 Dec 2009
Kida Miyuki, Tsutsumi Tomonori, Shindoh Masanobu, Ikeda Hisami, Ariga Tadashi
Abstract excerpt
Dentinogenesis imperfecta (DGI) type II is one of the most common dominantly inherited dentin defects, in which both the primary and permanent teeth are affected. Here, we report a Japanese family with autosomal-dominant DGI type II, including both molecular genetic defects and pathogenesis with...
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