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HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours
Background: Hyperparathyroidism is a common endocrinopathy characterised by the formation of parathyroid tumours. In this study, we determine the role of the recently identified gene, HRPT2, in parathyroid tumorigenesis. Methods: Mutation analysis of HRPT2 was undertaken in 60 parathyroid tumours: f...
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| 主要な著者: | , , , , , , , , , , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMJ Group
2003
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1735580/ https://ncbi.nlm.nih.gov/pubmed/12960210 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.40.9.657 |
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