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The impact of coexisting genetic mutations on murine optic glioma biology
BACKGROUND: Children with the neurofibromatosis type 1 (NF1) tumor predisposition syndrome are prone to the development of optic pathway gliomas resulting from biallelic inactivation of the NF1 gene. Recent studies have revealed the presence of other molecular alterations in a small portion of these...
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| Yayımlandı: | Neuro Oncol |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4482850/ https://ncbi.nlm.nih.gov/pubmed/25246427 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/nou287 |
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