Identification of Rare Variants in TNNI3 with Atrial Fibrillation in a Chinese GeneID Population

Despite advances by genome-wide association studies (GWAS), much of heritability of common human diseases remains missing, a phenomenon referred to as ‘missing heritability’. One potential cause for ‘missing heritability’ is the rare susceptibility variants overlooked by GWAS. Atrial fibrillation (A...

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Veröffentlicht in:Mol Genet Genomics
Hauptverfasser: Wang, Chuchu, Wu, Manman, Qian, Jin, Li, Bin, Tu, Xin, Xu, Chengqi, Li, Sisi, Chen, Shanshan, Zhao, Yuanyuan, Huang, Yufeng, Shi, Lisong, Cheng, Xiang, Liao, Yuhua, Chen, Qiuyun, Xia, Yunlong, Yao, Wei, Wu, Gang, Cheng, Mian, Wang, Qing K.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2015
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4713376/
https://ncbi.nlm.nih.gov/pubmed/26169204
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00438-015-1090-y
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