Published in
Oxford University Press (OUP), Human Molecular Genetics, 19(9), p. 2853-2858
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Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding Delta1-pyrroline-5-carboxylate synthase
Journal article published in 2000 by
M. R. Baumgartner 
This paper is made freely available by the publisher.
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