Succinic semialdehyde dehydrogenase deficiency—A further case
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01819287
Reference2 articles.
1. Gibson, K. M., Sweetman, L., Nyhan, W. L., Jakobs, C., Rating, D., Siemes, H. and Hanefeld, F. Succinic semialdehyde dehydrogenase deficiency: an inborn error of gamma-aminobutyric acid metabolism.Clin. Chim. Acta 133 (1983) 33–42
2. Jakobs, C., Bojasch, M., Monch, E., Rating, D., Siemes, H. and Hanefeld, F. Urinary excretion of gamma-hydroxybutyric acid in a patient with neurological abnormalities. The probability of a new inborn error of metabolism.Clin. Chim. Acta 111 (1981) 169–178
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