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

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

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...

Full description

Bibliographic Details
Main Authors: S Jalal Pourhashemi, Mehdi Ghandehari Motlagh, Ghasem Meighani, Azadeh Ebrahimi Takaloo, Mahsa Mansouri, Fatemeh Mohandes, Maryam Mirzaii, Ahad Khoshzaban, Faranak Moshtaghi, Hoda Abedkhojasteh, Mansour Heidari
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2014-12-01
Series:Iranian Journal of Public Health
Subjects:
Amelogenesis imperfecta
FAM83H
Iranian patients
Online Access:https://ijph.tums.ac.ir/index.php/ijph/article/view/3756

Similar Items

Similar Items