Amelogenesis Imperfecta and Screening of Mutation in Amelogenin Gene

The aim of this study was to report the clinical findings and the screening of mutations of amelogenin gene of a 7-year-old boy with amelogenesis imperfecta (AI). The genomic DNA was extracted from saliva of patient and his family, followed by PCR and direct DNA sequencing. The c.261C>T mutation...

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Detalhes bibliográficos
Main Authors: Oliveira, Fernanda Veronese, Gurgel, Carla Vecchione, Kobayashi, Tatiana Yuriko, Dionísio, Thiago José, Neves, Lucimara Teixeira, Santos, Carlos Ferreira, Machado, Maria Aparecida Andrade Moreira, Oliveira, Thais Marchini
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2014
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4089840/
https://ncbi.nlm.nih.gov/pubmed/25045544
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/319680
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