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Reyhaneh Seyfi

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Review Open access Sep 2026

Hyperammonemia: a review of etiologies, whole-exome sequencing diagnosis, and Iranian case reports

This review aims to provide a comprehensive overview of inherited metabolic disorders associated with hyperammonemia and to evaluate the diagnostic role of whole-exome sequencing (WES), with particular attention to Iranian patient data.

Reza Hajati, Sharareh Kamfar, Reyhaneh Seyfi et al. · 0 citations

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