Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1

• Главные авторы: Hossam Murad (Автор), Mohamad Baseel Alhalabi (Автор), Amir Dabboul (Автор), Nour Alfakseh (Автор), Mohamad Sayah Nweder (Автор), Youssef Zghib (Автор), Hala Wannous (Автор)
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• Опубликовано: BMC, 2021-06-01T00:00:00Z.
• Предметы: article
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Abstract Background Characterization of the molecular basis of primary hyperoxaluria type 1 (PH-1) in Syria has been accomplished through the analysis of 90 unrelated chromosomes from 45 Syrians patients with PH-1 from different regions. Methods Alanine glyoxylate aminotransferase (AGXT) gene mutati...