Genotype-Clinical Correlations in Polycystic Kidney Disease with No Apparent Family History

Conclusion: Detection ofPKD1/PKD2 mutation, especiallyPKD1 truncating, is useful for predicting the renal outcome and rate of TKV increase in PKD patients with no apparent family history.Am J Nephrol 2019;49:233 –240
Source: American Journal of Nephrology - Category: Neurology Source Type: research