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APC promoter 1B deletion in seven American families with familial adenomatous polyposis
Familial adenomatous polyposis (FAP) is a colorectal cancer predisposition syndrome caused by mutations in the adenomatous polyposis coli (APC) gene. Clinical genetic testing fails to identify disease causing mutations in up to 20% of clinically apparent FAP cases. Following the inclusion of multipl...
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| 發表在: | Clin Genet |
|---|---|
| Main Authors: | , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2014
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4732873/ https://ncbi.nlm.nih.gov/pubmed/25243319 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.12503 |
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