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Melanoma risk associated with p16 mutations was presented as a 35- to 70-fold increase from general population risk (approximately 1%) and illustrated with a bar graph indicating a risk of 50% by age 50 and 76% by age 80.
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Paclitaxel responses in relation to individual mutations are presented in Supporting Information Table S1.
Meanwhile, top seven hereditary retinal diseases with the highest number of related mutations are presented.
Reported IC50 values of clinically detected mutations are presented in Table 2 >.
Mutations are presented as an italicized superscript (e.g., rtls l1 ).
Summary of cell line mutations is presented in Supplementary Table 1.
Details of SCN1A mutations are presented in the Supplementary Tables 3 and 4.
In Fig. 5c, an example of mutation is presented.
Five cases with rare mutations and one case with novel mutation are presented in Table 2.
The genotypes for marker FCA931 and for the mutation are presented in Fig. 1.
Neither of these mutations was present in the germline.
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