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Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism

✍ Scribed by M. Duran; P. Rovers; P. K. de Bree; C. H. Schreuder; H. Beukenhorst; L. Dorland; R. Berger


Publisher
Springer
Year
1991
Tongue
English
Weight
274 KB
Volume
14
Category
Article
ISSN
0141-8955

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## Defects in man in four steps of 4aminobutyric acid (GABA) metabolism may interefere with the function of this major inhibitory neurotransmitter. Glutamic acid decarboxylase, 4-aminobutyric acid aminotransferase, succinic semialdehyde dehydrogenase, and homocarnosinase are closely identijied with