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Novel FAM83H mutations in patients with amelogenesis imperfecta
Amelogenesis imperfecta (AI), characterized by a deficiency in the quantity and/or quality of dental enamel, is genetically heterogeneous and phenotypically variable. The most severe type, hypocalcified AI, is mostly caused by truncating mutations in the FAM83H gene. This study aimed to identify gen...
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| 發表在: | Sci Rep |
|---|---|
| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Nature Publishing Group UK
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5519741/ https://ncbi.nlm.nih.gov/pubmed/28729668 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-05208-0 |
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