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Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15. [electronic resource] by
- Debray, F-G
- Lambert, M
- Lemieux, B
- Soucy, J F
- Drouin, R
- Fenyves, D
- Dubé, J
- Maranda, B
- Laframboise, R
- Mitchell, G A
Producer: 20081231
In:
Journal of medical genetics vol. 45
Availability: No items available.
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