The management and long term outcome of organic acidaemias
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF03047367
Reference3 articles.
1. Langenbeck, U., Wendel, U., Mench-Hoinowski, A., Kuschel, D., Becker, K., Przyrembel, H. and Bremer, H. J. Correlations between branched-chain amino acids and branched-chain α-keto acids in blood in maple syrup urine disease.Clin. Chitn. Acta 88 (1978) 283–291
2. Léonard, J. V., Seakins, J. W. T., Bartlett, K., Hyde, J., Wilson, J. and Clayton, B. Inherited disorders of 3-methylcrotonyl CoA carboxylation.Arch. Dis. Child. 56 (1981) 53–59
3. Naughten, E. R., Jenkins, J., Francis, D. E. M. and Leonard, J. V. Outcome of maple syrup urine disease.Arch. Dis. Child. 57 (1982) 918–921
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