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Hidden association of Cowden syndrome, PTEN mutation and meningioma frequency
Cowden syndrome (CS) is clinically presented by multiple hamartomas, often with mucocutaneous lesions, goiter, breast cancer and gastrointestinal polyps. CS is a genetic disorder of autosomal dominant inheritance and is one distinct syndrome of the phosphatase and tensin homolog on chromosome 10 (PT...
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| 出版年: | Oncoscience |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Impact Journals LLC
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4965257/ https://ncbi.nlm.nih.gov/pubmed/27489861 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncoscience.305 |
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