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

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

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...

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Bibliographic Details
Main Authors: Hossam Murad, Mohamad Baseel Alhalabi, Amir Dabboul, Nour Alfakseh, Mohamad Sayah Nweder, Youssef Zghib, Hala Wannous
Format: Article
Language:English
Published: BMC 2021-06-01
Series:BMC Medical Genomics
Subjects:
Primary hyperoxaluria type 1
AGXT
Syria
Online Access:https://doi.org/10.1186/s12920-021-00996-x

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