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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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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2009
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| Assuntos: | |
| 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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