Identification of 3 novel VHL germ-line mutations in Danish VHL patients
Research output: Contribution to journal › Journal article › Research › peer-review
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.
Original language | English |
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Journal | B M C Medical Genetics |
Volume | 13 |
Pages (from-to) | 54 |
ISSN | 1471-2350 |
DOIs | |
Publication status | Published - 2012 |
ID: 48529586