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Saf ve likit yaps sayesinde hzl etkileime girerek sporcularn definasyon ve kilo kontrol dnemlerinde en byk yardmclarndan biri olur

SLC22A5 mutations impair OCTN2 function, causing primary carnitine deficiency (PCD) ( Beyond genetic determinants, OCTN2 expression and function undergo significant physiological and pharmacological regulation

In the second case report, the infant showed acute mitochondrial encephalopathy, accompanied by increased level of lactate in the blood and cerebrospinal fluid as well as abnormal levels of -ketoglutarate in the urine

Or that is what we used to think

Psychiatry 64, 583588

cell in diabetes: Integrating biomarkers with functional measures