(Q46269021)
Statements
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Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15. (English)
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F-G Debray
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M Lambert
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B Lemieux
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J F Soucy
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R Drouin
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D Fenyves
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J Dubé
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B Maranda
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R Laframboise
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G A Mitchell
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1 November 2008
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45
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11
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759-764
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Identifiers
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