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An intronic variant in the CELF4 gene is associated with risk for colorectal cancer
BACKGROUND: Germline predisposition variants associated with colorectal cancer (CRC) have been identified but all are not yet identified. We sought to identify the responsible predisposition germline variant in an extended high-risk CRC pedigree that exhibited evidence of linkage to the 18q12.2 regi...
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| Publicado no: | Cancer Epidemiol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8158787/ https://ncbi.nlm.nih.gov/pubmed/33930674 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.canep.2021.101941 |
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