## Abstract Von Hippel‐Lindau (VHL) disease is an uncommon, autosomal dominant hereditary multitumor syndrome caused by germline alterations of the __VHL__ gene, which has been cloned recently and identified as a tumor suppressor gene. The major lesions in VHL disease include hemangioblastomas in t
✦ LIBER ✦
Von-Hippel-Lindau-Erkrankung
✍ Scribed by H. P. H. Neumann; M. Cybulla; S. Gläsker; C. Coulin; V. Van Velthoven; A. Berlis; C. Hader; O. Schäfer; M. Treier; I. Brink; W. Schultze-Seemann; C. Leiber; K. Rückauer; B. Junker; F. J. Agostini; A. Hetzel; C. C. Boedeker
- Publisher
- Springer Vienna
- Year
- 2007
- Tongue
- German
- Weight
- 754 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0930-4282
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von Hippel-Lindau (VHL) disease is an autosomal dominant familial cancer syndrome predisposing to the development of retinal and central nervous system haemangioblastomas, pheochromocytomas, renal and pancreatic cancer. In the course of a molecular analysis conducted to detect germline mutations of