organic acid

phosphoenolpyruvate carboxykinase 2, mitochondrial ; Homo sapiens







2 Article(s)
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Pub. Year
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1 28216384 Novel homozygous PCK1 mutation causing cytosolic phosphoenolpyruvate carboxykinase deficiency presenting as childhood hypoglycemia, an abnormal pattern of urine metabolites and liver dysfunction. 2017 Apr 1
2 26971250 Cytosolic phosphoenolpyruvate carboxykinase deficiency presenting with acute liver failure following gastroenteritis. 2016 May 1