Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia

Abstract Objectives Oligodontia is defined as the congenital absence of 6 or more permanent teeth excluding the third molar. The occurrence of non-syndromic still remains poorly understood, but in recent years some cases have been reported where mutations or polymorphisms of PAX9 and MSX1 had been a...

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