Missense Mutation in Fam83H Gene in Iranian Patients with Amelogenesis Imperfecta

BACKGROUND: 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 amelogenes...

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Detalles Bibliográficos
Autores principales: POURHASHEMI, S Jalal, GHANDEHARI MOTLAGH, Mehdi, MEIGHANI, Ghasem, EBRAHIMI TAKALOO, Azadeh, MANSOURI, Mahsa, MOHANDES, Fatemeh, MIRZAII, Maryam, KHOSHZABAN, Ahad, MOSHTAGHI, Faranak, ABEDKHOJASTEH, Hoda, HEIDARI, Mansour
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499090/
https://www.ncbi.nlm.nih.gov/pubmed/26171361

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499090/
https://www.ncbi.nlm.nih.gov/pubmed/26171361

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