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

• 主要な著者: Hossam Murad (著者), Mohamad Baseel Alhalabi (著者), Amir Dabboul (著者), Nour Alfakseh (著者), Mohamad Sayah Nweder (著者), Youssef Zghib (著者), Hala Wannous (著者)
• フォーマット: 図書
• 出版事項: BMC, 2021-06-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

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...