Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: CHCHD1[original query] |
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Sequence variants in four candidate genes (NIPSNAP1, GBAS, CHCHD1 and METT11D1) in patients with combined oxidative phosphorylation system deficiencies. Journal of inherited metabolic disease 2010 S13-9. Smits P, Rodenburg R J, Smeitink J A M, van den Heuvel L |
Integration of summary data from GWAS and eQTL studies identified novel risk genes for coronary artery disease. Medicine 2021 Mar 100 (11): e24769. Zhong Yigang, Chen Liuying, Li Jingjing, Yao Yinghao, Liu Qiang, Niu Kaimeng, Ma Yunlong, Xu Yizh |
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- Page last updated:Apr 16, 2024
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