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Mutation of von Hippel[ndash ]Lindau tumor suppressor gene in a sporadic endolymphatic sac tumor

✍ Scribed by Shuji Hamazaki; Minoru Yoshida; Masahiro Yao; Yoji Nagashima; Kohji Taguchi; Hiroyuki Nakashima; Shigeru Okada

Book ID
117818521
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
221 KB
Volume
32
Category
Article
ISSN
1532-8392

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Communicated by Victor A. McKusick von Hippel-Lindau disease (VHL) is an inherited neoplastic disorder characterized by the development of tumors in the eyes, brain, spinal cord, inner ear, adrenal gland, pancreas, kidney, and epididymis. The VHL tumor suppressor gene was identified in 1993. Initial