The autosomal recessive oxalosis 3 is hyperoxaluria, oxalate nephrolithiasis and nephrocalcinosis due to mutations of the HOGA1 gene.
1. |
Belostotsky R et al. (2010) Mutations in DHDPSL are responsible for primary hyperoxaluria type III. |
2. |
OMIM.ORG article Omim 613616 |