Hyperammonemia with reduced ornithine, citrulline, arginine and proline: A new inborn error caused by a mutationin in the gene encoding Δ1-pyrroline-5-carboxylate synthase
Matthias R. Baumgartner, Chien An A. Hu, Shlomo Almashanu, Gary Steel, Cassandra Obie, Bernard Aral, Daniel Rabier, Pierre Kamoun, Jean Marie Saudubray, David Valle
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