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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499090/ https://www.ncbi.nlm.nih.gov/pubmed/26171361 |
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