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

• Main Authors: Hossam Murad (Author), Mohamad Baseel Alhalabi (Author), Amir Dabboul (Author), Nour Alfakseh (Author), Mohamad Sayah Nweder (Author), Youssef Zghib (Author), Hala Wannous (Author)
• Format: Book
• Published: BMC, 2021-06-01T00:00:00Z.
• Subjects: article
• Online Access: 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...