Abstract
The rare variant hypothesis postulates that genetic susceptibility to colorectal neoplasia within the general population is due to a number of low frequency variants in a variety of different genes. Each variant confers a moderate, but detectable, increase in relative risk of developing the disease. Recent evidence suggests that a quarter of patients with multiple adenomatous polyps are due to rare but functionally important variants in just five genes. ©2005 Landes Bioscience.
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Fearnhead, N. S., Winney, B., & Bodmer, W. F. (2005). Rare variant hypothesis for multifactorial inheritance: Susceptibility to colorectal adenomas as a model. Cell Cycle. Taylor and Francis Inc. https://doi.org/10.4161/cc.4.4.1591
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