Article
[Hereditary diseases with tooth anomalies and their causal genes].
Kaibogaku zasshi. Journal of anatomy - 1 Jun 1998
Kurisu K, Tabata M J
Abstract excerpt
In this review, we describe the current knowledge and the advances in research on human genes whose defect leads to dental anomalies. Recently, it was demonstrated that a missense mutation of a human homeobox MSX1 gene causes autosomal dominant agenesis of second premolars and third molars. X-lin...
Topics
- Alkaline Phosphatase
- Amelogenin
- Collagen
- Dental Enamel Proteins
- Dentinogenesis Imperfecta
- Genes, Homeobox
- Humans
- Hypophosphatasia
- Membrane Proteins
- Mutation
- Tooth Abnormalities