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ArticleJournal of inherited metabolic disease2024

Use of pure recombinant human enzymes to assess the disease-causing potential of missense mutations in urea cycle disorders, applied to N-acetylglutamate synthase deficiency.

Nadine Gougeard et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2024
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Full record →Abstract, authors, funding and every citing paper · PMID 38740568