Identification of 3 novel VHL germ-line mutations in Danish VHL patients
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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 VHL gene.
Originalsprog | Engelsk |
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Tidsskrift | B M C Medical Genetics |
Vol/bind | 13 |
Sider (fra-til) | 54 |
ISSN | 1471-2350 |
DOI | |
Status | Udgivet - 2012 |
ID: 48529586