GRHPR gene mutation

Clinical significance

• GRHPR gene mutations are the cause of primary hyperoxaluria type 2

More general terms

• gene mutation testing; gene mutation analysis

Additional terms

• glyoxylate reductase/hydroxypyruvate reductasel D-glycerate dehydrogenase; D-glyceric dehydrogenase (GRHPR, GLXR, MSTP035)