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Published in 2017 at "Human Mutation"
DOI: 10.1002/humu.23163
Abstract: Single‐nucleotide variants (SNVs) are the most frequent genetic changes found in human cancer. Most driver alterations are missense and nonsense variants localized in the coding region of cancer genes. Unbiased cancer genome sequencing shows that…
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Keywords:
cancer infamous;
human cancer;
somatic variants;
synonymous somatic ... See more keywords