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VHL |
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nbsp;that are associated with von Hippel-Lindau (VHL) disease. 2][mu]-globulin, peroxisome proliferation, oxidative stress, nephrotoxicity/cytotoxicity (including the role of formic acid), and the potential role of mutations in the von Hippel-Lindau tumor (VHL) suppressor gene (U. More than 40 neurocutaneous syndromes have been described, the most common of which are neurofibromatosis I and II, tuberous sclerosis, Sturge-Weber syndrome, and von Hippel-Lindau syndrome. |
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