. . . . . "ALDH18A1" . . . . "Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding delta(1)-pyrroline-5-carboxylate synthase" . . . . "2018-04-05T10:17:11.353+02:00"^^ . . . . . .