Search
GRHPR gene mutation
Clinical significance:
- GRHPR gene mutations are the cause of primary hyperoxaluria type 2
Related
glyoxylate reductase/hydroxypyruvate reductasel D-glycerate dehydrogenase; D-glyceric dehydrogenase (GRHPR, GLXR, MSTP035)
General
gene mutation testing; gene mutation analysis
References
Loinc