## Abstract Von Hippel–Lindau (VHL) disease type 2A is an inherited tumor syndrome characterized by predisposition to pheochromocytoma (pheo), retinal hemangioma (RA), and central nervous system hemangioblastoma (HB). Specific VHL subtypes display genotype–phenotype correlations but, unlike other f
✦ LIBER ✦
Somatic mutations in VHL germline deletion kindred correlate with mild phenotype
✍ Scribed by Scott D. Wait; Alexander O. Vortmeyer; Russell R. Lonser; David T. Chang; Michael A. Finn; Deb A. Bhowmick; Svetlana D. Pack; Edward H. Oldfield; Zhengping Zhuang
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 386 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0364-5134
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