Recurrent, low-frequency coding variants contributing to colorectal cancer in the Swedish population.

Genome-wide association studies (GWAS) have identified dozens of common genetic variants associated with risk of colorectal cancer (CRC). However, the majority of CRC heritability remains unclear. In order to discover low-frequency, high-risk CRC susceptibility variants in Swedish population, we gen...

Täydet tiedot

Bibliografiset tiedot

Päätekijät:	Xiang Jiao, Wen Liu, Hovsep Mahdessian, Patrick Bryant, Jenny Ringdahl, Maria Timofeeva, Susan M Farrington, Malcolm Dunlop, Annika Lindblom
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Public Library of Science (PLoS) 2018-01-01
Sarja:	PLoS ONE
Linkit:	https://doi.org/10.1371/journal.pone.0193547
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