Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding Δ 1 -pyrroline-5-carboxylate synthase

Author： Baumgartner Matthias R.  

Publisher： Oxford University Press

E-ISSN： 0964-6906|9|19|2853-2858

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.9, Iss.19, 2000-11, pp. : 2853-2858

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