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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. [electronic resource] by
- Baumgartner, M R
- Hu, C A
- Almashanu, S
- Steel, G
- Obie, C
- Aral, B
- Rabier, D
- Kamoun, P
- Saudubray, J M
- Valle, D
Producer: 20010103
In:
Human molecular genetics vol. 9
Availability: No items available.
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Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. [electronic resource] by
- Camacho, J A
- Obie, C
- Biery, B
- Goodman, B K
- Hu, C A
- Almashanu, S
- Steel, G
- Casey, R
- Lambert, M
- Mitchell, G A
- Valle, D
Producer: 19990629
In:
Nature genetics vol. 22
Availability: No items available.
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15.
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Short-term supplementation of isocaloric meals with L-tryptophan affects pig growth. [electronic resource] by
- Liu, H N
- Hu, C-A A
- Bai, M M
- Liu, Gang
- Tossou, M C B
- Xu, K
- Li, F N
- Liao, P
- Kong, X F
- Wu, X
- Yin, Y L
Producer: 20181119
In:
Amino acids vol. 49
Availability: No items available.
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