Identification of 3 novel <it>VHL</it> germ-line mutations in Danish VHL patients

• Main Authors: Dandanell Mette (Author), Friis-Hansen Lennart (Author), Sunde Lone (Author), Nielsen Finn C (Author), Hansen Thomas (Author)
• Format: Book
• Published: BMC, 2012-07-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<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 caus...