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Synchronous Presentation of Rare Brain Tumors in Von Hippel–Lindau Syndrome
Von Hippel–Lindau (VHL) disease is a heritable cancer syndrome in which benign and malignant tumors and/or cysts develop throughout the central nervous system (CNS) and visceral organs. The disease results from mutations in the VHL tumor suppressor gene located on chromosome 3 (3p25-26). A majority...
Guardat en:
| Publicat a: | Diagnostics (Basel) |
|---|---|
| Autors principals: | , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8228671/ https://ncbi.nlm.nih.gov/pubmed/34072835 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diagnostics11061005 |
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