Published in Cancer Weekly, February 25th, 2003
This discovery has promising therapeutic implications for the treatment of neurofibromatosis type 1 (NF1), a common hereditary disease that results from mutations in the neurofibromin gene, as well as the approximately 30% of human tumors that have altered Ras activity.
The report is published in the February 15, 2003, issue of Genes & Development.
Neurofibromin is a tumor...
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Source: Cancer Weekly (2003-02-25)
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