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Advances in clinical chemistry , 87 , 141159
Rare mutations in the SLC22A5 gene can cause a genetic condition called primary carnitine deficiency, which is usually discovered in infancy because it affects brain function, muscle function, and blood glucose levels
These drugs do the same thing
Since mesenchymal lines typically originate from invasive and metastatic tumors, our results suggest that reduction of SAA metabolism genes and the consequent rewiring of SAA metabolism may represent hallmarks of liver cancer progression
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