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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,...
Tallennettuna:
| Julkaisussa: | Neurooncol Adv |
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| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2020
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| Aiheet: | |
| Linkit: | 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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