Germline variants in the Von Hippel-Lindau tumor suppressor gene in Cuban patients
Abstract Background Von Hippel-Lindau (VHL) syndrome is an autosomal dominantly inherited disorder that predisposes to multiple neoplasms. Patients may develop hemangioblastomas of the central nervous system and retina, multiple cysts in the pancreas and kidneys, renal carcinoma, and pheochromocytom...
Furkejuvvon:
| Váldodahkkit: | , , , |
|---|---|
| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
SpringerOpen
2024-03-01
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| Ráidu: | Egyptian Journal of Medical Human Genetics |
| Fáttát: | |
| Liŋkkat: | https://doi.org/10.1186/s43042-024-00506-5 |
| Fáddágilkorat: |
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