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Cutaneous neurofibromas in the genomics era: current understanding and open questions
Cutaneous neurofibromas (cNF) are a nearly ubiquitous symptom of neurofibromatosis type 1 (NF1), a disorder with a broad phenotypic spectrum caused by germline mutation of the neurofibromatosis type 1 tumour suppressor gene (NF1). Symptoms of NF1 can include learning disabilities, bone abnormalities...
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| 出版年: | Br J Cancer |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group UK
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6008439/ https://ncbi.nlm.nih.gov/pubmed/29695767 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41416-018-0073-2 |
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