Germline EPHB2 receptor variants in familial colorectal cancer.
Familial clustering of colorectal cancer occurs in 15-20% of cases, however recognized cancer syndromes explain only a small fraction of this disease. Thus, the genetic basis for the majority of hereditary colorectal cancer remains unknown. EPHB2 has recently been implicated as a candidate tumor sup...
Päätekijät: | , , , , , , , , , , , |
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Aineistotyyppi: | Artikkeli |
Kieli: | English |
Julkaistu: |
Public Library of Science (PLoS)
2008-08-01
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Sarja: | PLoS ONE |
Linkit: | http://europepmc.org/articles/PMC2483346?pdf=render |