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...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Jiao, Xiang, Liu, Wen, Mahdessian, Hovsep, Bryant, Patrick, Ringdahl, Jenny, Timofeeva, Maria, Farrington, Susan M., Dunlop, Malcolm, Lindblom, Annika
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2018
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5856271/
https://ncbi.nlm.nih.gov/pubmed/29547645
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0193547
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