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Article

ABCC4 copy number variation is associated with susceptibility to esophageal squamous cell carcinoma.

Carcinogenesis - 1 Sept 2014

Sun Yulin, Shi Ni, Lu Haizhen, Zhang Jinqiang, Ma Yulong, Qiao Yuanyuan, Mao Yonghong, Jia Kun, Han Lifen, Liu Fang, Li Hongxia, Lin Zhengwei, Li Xinmin, Zhao Xiaohang

Abstract excerpt

Esophageal squamous cell carcinoma (ESCC) is the eighth most common cause of cancer-related death worldwide. However, previous genome-wide single nucleotide polymorphism association analyses have not explained the high heritability associated with ESCC. In this study, we performed genome-wide copy number variation (CNV) analysis on 128 discordant sibling pairs to identify novel genes that contribute to ESCC...

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Share to Carcinoma, Squamous Cell
Share to Chromosomes, Human, Pair 13

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Enhancer Elements, Genetic

Share to Esophageal Neoplasms

Share to Gene Dosage

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Source

Identifiers

PMID: 24510239
DOI: 10.1093/carcin/bgu043

Genes

ABCC4

Provenance

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