Publications
Clinical characteristics, genetic profile and short-term outcomes of children with primary hyperoxaluria type 2: a nationwide experience
Krishnasamy S, Deepthi B, Kamath N, Iyengar A, Thomas CC, Uthup S, Saha A, Mathew G, Agarwal I, Tiewsoh K, Bhat NK, Mandal K, Krishnamurthy S Three types of primary hyperoxaluria (PH) are recognized. However, data on PH type 2 (PH2), caused by defects in the GRHPR gene, are limited.
