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HYPEROXALURIA, PRIMARY, TYPE III

Known as: HP3, Primary Hyperoxaluria Type III 
Recessively inherited primary hyperoxaluria due to mitochondrial 4-hydroxy-2-oxoglutarate aldolase (HOGA1) gene mutations.(NICHD)
National Institutes of Health

Papers overview

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2019
2019
FLOW AND PHYSICAL PROPERTIES PROBE (HP) MOLE AS A SEISMIC SOURCE S. Kedar, W. B. Banerdt, N. Brinkman, P. Delage, L. Fayon, M… 
2017
2017
Significant changes in global climate and carbon cycling occurred during the Early Cretaceous. This study examines the expression… 
Review
2016
Review
2016
This paper provides a description of the specific design features and nuances of the Hammering Mechanism, a drive unit for the… 
Review
2016
Review
2016
An overview of the development and the qualification process of the Support System is presented. The relevant requirements, the… 
2014
2014
Uberblick uber das Radiometer des Heat Flow and Physical Properties Packages (HP3) der InSight Mission. 
2003
2003
Summary. Experimental and clinical studies have shown that HAp granules and powder may be successfully applied in reconstruction… 
2002
2002
Extracellular enzymes secreted by Zoogloea itzigohn HP3 belong to component enzymes, which could decolor ABAS and the optimum… 
1977
1977
Bacteriophage phi 29 mutation sus8(22) has been mapped by two-factor crosses between markers sus8(769) and ts8(93). Whe sus8(22…