Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
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. 
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| 2. |
OMIM.ORG article Omim 613616
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