Missense Mutation in Fam83H Gene in Iranian Patients with Amelogenesis Imperfecta.

• Main Authors: S Jalal Pourhashemi (Author), Mehdi Ghandehari Motlagh (Author), Ghasem Meighani (Author), Azadeh Ebrahimi Takaloo (Author), Mahsa Mansouri (Author), Fatemeh Mohandes (Author), Maryam Mirzaii (Author), Ahad Khoshzaban (Author), Faranak Moshtaghi (Author), Hoda Abedkhojasteh (Author), Mansour Heidari (Author)
• Format: Book
• Published: Tehran University of Medical Sciences, 2014-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Amelogenesis Imperfecta (AI) is a disorder of tooth development where there is an abnormal formation of enamel or the external layer of teeth. The aim of this study was to screen mutations in the four most important candidate genes, ENAM, KLK4, MMP20 and FAM83H responsible for amelogenesis imperfect...