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Deletion of amelotin exons 3–6 is associated with amelogenesis imperfecta
Amelogenesis imperfecta (AI) is a heterogeneous group of genetic conditions that result in defective dental enamel formation. Amelotin (AMTN) is a secreted protein thought to act as a promoter of matrix mineralization in the final stage of enamel development, and is strongly expressed, almost exclus...
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| 發表在: | Hum Mol Genet |
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| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Oxford University Press
2016
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5179951/ https://ncbi.nlm.nih.gov/pubmed/27412008 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw203 |
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