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In:
Molecular genetics and metabolism vol. 103
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In:
Journal of inherited metabolic disease vol. 35
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N-Acetylglutamate Synthase Deficiency Due to a Recurrent Sequence Variant in the N-acetylglutamate Synthase Enhancer Region. [electronic resource] by
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In:
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Dual mechanism of brain damage induced in vivo by the major metabolites accumulating in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome. [electronic resource] by
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- Schuck, Patrícia Fernanda
- Ferreira, Gustavo da Costa
- Sitta, Angela
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Urea cycle disorders in Argentine patients: clinical presentation, biochemical and genetic findings. [electronic resource] by
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- Bezard, Miriam
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Producer: 20200427
In:
Orphanet journal of rare diseases vol. 14
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