2 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
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 |