Phenotypic Variation in FAM83H-associated Amelogenesis Imperfecta

FAM83H gene mutations are associated with autosomal-dominant hypocalcified amelogenesis imperfecta (ADHCAI), which is typically characterized by enamel having normal thickness and a markedly decreased mineral content. This study tested the hypothesis that there are phenotype and genotype association...

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Detalhes bibliográficos
Principais autores: Wright, J.T., Frazier-Bowers, S., Simmons, D., Alexander, K., Crawford, P., Han, S.T., Hart, P.S., Hart, T.C.
Formato: Artigo
Idioma:Inglês
Publicado em: SAGE Publications 2009
Assuntos:
Research Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2754853/
https://ncbi.nlm.nih.gov/pubmed/19407157
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034509333822
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