APA

Baumgartner M. R., Hu C. A., Almashanu S., Steel G., Obie C., Aral B., Rabier D., Kamoun P., Saudubray J. M. & Valle D. (20010103). 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. : Human molecular genetics.

Chicago

Baumgartner M R, Hu C A, Almashanu S, Steel G, Obie C, Aral B, Rabier D, Kamoun P, Saudubray J M and Valle D. 20010103. 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. : Human molecular genetics.

Harvard

Baumgartner M. R., Hu C. A., Almashanu S., Steel G., Obie C., Aral B., Rabier D., Kamoun P., Saudubray J. M. and Valle D. (20010103). 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. : Human molecular genetics.

MLA

Baumgartner M R, Hu C A, Almashanu S, Steel G, Obie C, Aral B, Rabier D, Kamoun P, Saudubray J M and Valle D. 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. : Human molecular genetics. 20010103.