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The Molecular Etiologies and Associated Phenotypes of Amelogenesis Imperfecta

The amelogenesis imperfectas (AIs) are a clinically and genetically diverse group of conditions that are caused by mutations in a variety of genes that are critical for normal enamel formation. To date, mutations have been identified in four genes (AMELX, ENAM, KLK4, MMP20) known to be involved in e...

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Detalhes bibliográficos
Autor principal: Wright, J. Timothy
Formato: Artigo
Idioma:Inglês
Publicado em: 2006
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1847600/
https://ncbi.nlm.nih.gov/pubmed/16838342
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.31358
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