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Exploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromas
Neurofibromatosis type-1 (NF1), caused by heterozygous inactivation of the NF1 tumour suppressor gene, is associated with the development of benign and malignant peripheral nerve sheath tumours (MPNSTs). Although numerous germline NF1 mutations have been identified, relatively few somatic NF1 mutati...
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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: |
Nature Publishing Group
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3306856/ https://ncbi.nlm.nih.gov/pubmed/22108604 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.207 |
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