A Review of Von Hippel-Lindau Syndrome
<p>Von Hippel-Lindau syndrome (VHL) is a familial neoplastic condition seen in approximately 1 in 36,000 live births. It is caused by germline mutations of the tumor suppressor gene VHL, located on the short arm of chromosome 3. While the majority of the affected individuals have a positive fa...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Codon Publications
2017-08-01
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| Series: | Journal of Kidney Cancer and VHL |
| Subjects: | |
| Online Access: | https://jkcvhl.com/index.php/jkcvhl/article/view/88 |