ロード中...
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma
Mutations in two genes encoding cell cycle regulatory proteins have been shown to cause familial cutaneous malignant melanoma (CMM). About 20% of melanoma-prone families bear a point mutation in the CDKN2A locus at 9p21, which encodes two unrelated proteins, p16(INK4a) and p14(ARF). Rare mutations i...
保存先:
| 主要な著者: | , , , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group
2008
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2480975/ https://ncbi.nlm.nih.gov/pubmed/18612309 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjc.6604470 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|