Mitochondrial phosphoenolpyruvate carboxykinase deficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF01963566.pdf
Reference6 articles.
1. Atkin BM, Utter MF, Weinberg MB (1979) Pyruvate carboxylase and phosphoenol pyruvate carboxykinase activity in leucocytes and fibroblasts from a patient with pyruvate carboxylase deficiency. Pediatr Res 13:38–43
2. Clayton PT, Hyland K, Brand M, Leonard JV (1986) Mitochondrial phosphoenol pyruvate carboxykinase deficiency. Eur J Pediatr 145:46–50
3. DiMauro S, Nicholson JF, Hays AP, Eastwood AB, Papadimitrou A, Koenigsberger R, De Vivo DC (1983) Benign infantile mitochondrial myopathy due to reversible cytochrome oxidase deficiency. Ann Neurol 14:226–234
4. Hyland K, Leonard JV (1983) Revised assays for the investigation of congenital lactic acidoses using14C keto acids, eliminating the problem of spontaneous decarboxylation. Clin Chim Acta 133:177–187
5. King TE, Howard RL (1967) Preparation and properties of soluble NADH dehydrogenases from cardiac muscle. Methods Enzymol Volume X:275–294
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