| Literature DB >> 24103583 |
Sofia I N Lopez1, Karina S Mundstock, Vanessa R Paixão-Côrtes, Lavínia Schüler-Faccini, Carlos A Mundstock, Maria Cátira Bortolini, Francisco M Salzano.
Abstract
Non-syndromic agenesis of permanent teeth is one of the most common anomalies in human development, a multifactorial characteristic caused by genetic and environmental factors. We describe a pair of monozygotic twins who showed second premolar and third molar agenesis, albeit with different expressions. We studied the DNA of two genes, paired domain box gene 9 (PAX9) and muscle segment homeodomain-homeobox1 (MSX1), encoding transcription factors that earlier studies found were involved in the manifestation of this condition. No specific causative mutation was found. However, we detected a C→T change in MSX1 exon 2 in both twins, suggesting that this polymorphism might be involved in the trait's expression.Entities:
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Year: 2013 PMID: 24103583 DOI: 10.1017/thg.2013.69
Source DB: PubMed Journal: Twin Res Hum Genet ISSN: 1832-4274 Impact factor: 1.587