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Paper Details

Citrin/mitochondrial glycerol-3-phosphate dehydrogenase double knock-out mice recapitulate features of human citrin deficiency.
J Biol Chem
61
2007
/, Citrin, NAD(+), NADH, SLC25A13 gene, aspartate, citrin, citrin deficiency, citrullinemia, cytosol, fatty liver, glutamate, glycerol 3-phosphate, glycerol phosphate, glycerol-3-phosphate, human, humans, hyperammonemia, hypoglycemia, lactate, liver-type mitochondrial aspartate-glutamate carrier, malate, mice, mitochondrial glycerol 3-phosphate dehydrogenase, mitochondrial glycerol-3-phosphate dehydrogenase, mouse, neonatal intrahepatic cholestasis, nucleotide, pyruvate, sucrose, type II citrullinemia, urea

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