Methylmalonyl-CoA mutase (EC 5.4.99.2) is a mitochondrial matrix enzyme whose activity is deficient in the inherited disorder methylmalonic acidemia. Previous studies on primary fibroblast cell lines

PubMed Central30

Additional file 10: of Studies of liver tissue identify functional gene regulatory elements associated to gene expression, type 2 diabetes, and other metabolic diseases

肝脏基因组学

代谢疾病分子机制

Table S6. Results of the funMotifs analysis. (XLSX 16 kb)

Figshare2019-04-30 更新20

Adiponectin receptor 1 expression.

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