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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Detalles Bibliográficos
Autores principales: Dare, Anna J, Gupta, Abha A, Thipphavong, Seng, Miettinen, Markku, Gladdy, Rebecca A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Supplement Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317050/
https://www.ncbi.nlm.nih.gov/pubmed/32642738
http://dx.doi.org/10.1093/noajnl/vdaa032

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317050/
https://www.ncbi.nlm.nih.gov/pubmed/32642738
http://dx.doi.org/10.1093/noajnl/vdaa032

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