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Whole-genome sequencing identifies new genetic alterations in meningiomas
The major known genetic contributor to meningioma formation was NF2, which is disrupted by mutation or loss in about 50% of tumors. Besides NF2, several recurrent driver mutations were recently uncovered through next-generation sequencing. Here, we performed whole-genome sequencing across 7 tumor-no...
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| Vydáno v: | Oncotarget |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Impact Journals LLC
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5370023/ https://ncbi.nlm.nih.gov/pubmed/28177878 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.15043 |
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