Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene

Overview of attention for article published in Frontiers in Genetics, November 2022

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HHH syndrome in patients from Palestine @aaup_edu @imad Dweikat

24 Nov 2022

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New Research: Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene: Background:… https://t.co/96fin35Xai #Genetics

24 Nov 2022

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