Germline mutations in the von Hippel–Lindau gene in Italian patients
✍ Scribed by Paola Ciotti; Anna Garuti; Rossella Gulli; Alberto Ballestrero; Emilia Bellone; Paola Mandich
- Book ID
- 116433198
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 111 KB
- Volume
- 52
- Category
- Article
- ISSN
- 1769-7212
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📜 SIMILAR VOLUMES
Communicated by Victor A. McKusick von Hippel-Lindau disease (VHL) is an inherited neoplastic disorder characterized by the development of tumors in the eyes, brain, spinal cord, inner ear, adrenal gland, pancreas, kidney, and epididymis. The VHL tumor suppressor gene was identified in 1993. Initial
## Communicated by Lap-Chee Tsui Von Hippel-Lindau (VHL) disease is a dominantly inherited disorder predisposing those afflicted to hemangioblastomas of the central nervous system and the retina, renal cell carcinomas, pheochromocytomas, and pancreatic tumors. The disease has been associated with