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Identification of novel mutations by exome sequencing in African American colorectal cancer patients
BACKGROUND: To identify genome wide single nucleotide variants (SNVs) and mutations in African Americans (AAs) with colorectal cancer (CRC). There is a need of such studies in AAs since they display a higher incidence of aggressive CRC tumors. METHODS: We performed whole exome sequencing (WES) on DN...
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| Publicado no: | Cancer |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4296906/ https://ncbi.nlm.nih.gov/pubmed/25250560 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cncr.28922 |
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