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Recurrent Coding Sequence Variation Explains only A Small Fraction of the Genetic Architecture of Colorectal Cancer

Recurrent Coding Sequence Variation Explains only A Small Fraction of the Genetic Architecture of Colorectal Cancer

10.1038/srep16286

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書目詳細資料
Main Authors: Timofeeva, M.N, Kinnersley, B, Farrington, S.M
其他作者: DUKE-NUS MEDICAL SCHOOL
格式: Article
出版: Nature Publishing Group 2020
主題:
activating transcription factor 1
ATF1 protein, human
cadherin
LNK protein, human
protein
allele
case control study
Caucasian
colorectal tumor
gene frequency
gene linkage disequilibrium
genetic variation
genetics
genome-wide association study
genotype
human
odds ratio
pathology
single nucleotide polymorphism
Activating Transcription Factor 1
Alleles
Cadherins
Case-Control Studies
Colorectal Neoplasms
European Continental Ancestry Group
Gene Frequency
Genetic Variation
Genome-Wide Association Study
Genotype
Humans
Linkage Disequilibrium
Odds Ratio
Polymorphism, Single Nucleotide
Proteins
在線閱讀:https://scholarbank.nus.edu.sg/handle/10635/180418
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https://scholarbank.nus.edu.sg/handle/10635/180418

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