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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Pubblicato in:Iran J Public Health
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: Tehran University of Medical Sciences 2014
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Original Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4499090/
https://ncbi.nlm.nih.gov/pubmed/26171361
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