Identification of 3 novel <it>VHL</it> germ-line mutations in Danish VHL patients
<p>Abstract</p> <p>Background</p> <p>von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome in which the patients develop retinal and central nervous system hemangioblastomas, pheochromocytomas and clear-cell renal tumors. The autosomal dominant disease is caused by mutations in the <it>VHL...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BMC
2012-07-01
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| Cyfres: | BMC Medical Genetics |
| Pynciau: | |
| Mynediad Ar-lein: | http://www.biomedcentral.com/1471-2350/13/54 |
| Tagiau: |
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