Fig. 2From: Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1a–f Sequence chromatograms of the c.198C > A (p.Tyr66X), c.305 T > A (p.Val102Asp), c.602A > T (p. Asp201Val), c.359-1_382del, c.941C > T (p.Pro314Leu) and c.140G > A (p.Gly47Glu) mutations in the AGXT gene. Arrow shows the sequence changeBack to article page