Lactic acidaemia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF03047378
Reference40 articles.
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2. Bartlett, K. and Gompertz, D. Biotin activation of carboxylase activity in cultured fibroblasts from a child with combined carboxylase defect.Clin. Chim. Acta 84 (1978) 399–401
3. Bartlett, K., Ghneim, H. K., Stirk, J.-H., Dale, G. and Alberti, K. G. M. M. Pyruvate carboxylase deficiency.J. Inker. Metab. Dis. 7, Suppl. 1 (1984) 74–78
4. Blass, J. P., Avigan, J. and Uhlendorf, B. W. A defect in pyruvate decarboxylase in a child with an intermittent movement disorder.J. Clin. Invest. 49 (1970) 423
5. Blass, J. P., Kark, R. A. P. and Engel, W. K. Clinical studies of a patient with pyruvate decarboxylase deficiency.Arch. Neurol. 25 (1971a) 449–460
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