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Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1 microdeletions
BACKGROUND: Neurofibromatosis type-1 (NF1) is caused by mutations of the NF1 gene at 17q11.2. In 95% of non-founder NF1 patients, NF1 mutations are identifiable by means of a comprehensive mutation analysis. 5-10% of these patients harbour microdeletions encompassing the NF1 gene and its flanking re...
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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: |
BioMed Central
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3500256/ https://ncbi.nlm.nih.gov/pubmed/23101500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-13-98 |
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