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Abdominal neoplastic manifestations of neurofibromatosis type 1
Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary tumor syndrome, with a wide clinicopathologic spectrum. It is defined by characteristic central nervous system, cutaneous and osseous manifestations, and by mutations in the NF1 gene, which is involved in proliferation via p21, RAS,...
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| Publicat a: | Neurooncol Adv |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7317050/ https://ncbi.nlm.nih.gov/pubmed/32642738 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/noajnl/vdaa032 |
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