by specific mutations in the NF1
gene (causing substitutions of amino acids in neurofibromin: p.Arg1038, p
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gene methylation level in patients with different clinical parameters, including the stage of disease
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different SNPs, most of which are located in intronic and intergenic regions where
genes encoding
1C, GABBR2, TCF7L2, DCK, NRP1, PBX1, FANCC, CCDC88C, TCF12, and ABLIM1
genes. Prevention
Retroelements occupy 37% of the human genome and are involved in the regulation of
gene expression
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gene