4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22771891&form=6&db=m 4-Hydroxy-2-oxoglutarate aldolase inactivity in primary hyperoxaluria type 3 and glyoxylate reductase inhibition. diagnostic usage,unassigned 2,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27096395&form=6&db=m Cellular degradation of 4-hydroxy-2-oxoglutarate aldolase leads to absolute deficiency in primary hyperoxaluria type 3. causal interaction,unassigned 4,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33543760&form=6&db=m Clinical characterization of primary hyperoxaluria type 3 in comparison to types 1 and 2: a retrospective cohort study. causal interaction,unassigned 4,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28271480&form=6&db=m Dihydrodipicolinate Synthase: Structure, Dynamics, Function, and Evolution. therapeutic application,unassigned 3,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29071511&form=6&db=m Folding Defects Leading to Primary Hyperoxaluria. therapeutic application,unassigned 1,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27561601&form=6&db=m HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients. causal interaction,diagnostic usage,unassigned 4,1,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26428388&form=6&db=m Hydroxyproline metabolism in a mouse model of Primary Hyperoxaluria Type 3. causal interaction,therapeutic application,unassigned 4,1,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31401635&form=6&db=m Mutation Hot Spot Region in the HOGA1 Gene Associated with Primary Hyperoxaluria Type 3 in the Chinese Population. unassigned - 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20797690&form=6&db=m Mutations in DHDPSL are responsible for primary hyperoxaluria type III. causal interaction,unassigned 3,0 4.1.3.16 Hyperoxaluria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33350326&form=6&db=m Mutations in HOGA1 do Not Confer a Dominant Phenotype Manifesting as Kidney Stone Disease. causal interaction,ongoing research,unassigned 4,3,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33350326&form=6&db=m Mutations in HOGA1 do Not Confer a Dominant Phenotype Manifesting as Kidney Stone Disease. causal interaction,ongoing research,unassigned 4,3,0 4.1.3.16 Kidney Calculi http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33350326&form=6&db=m Mutations in HOGA1 do Not Confer a Dominant Phenotype Manifesting as Kidney Stone Disease. causal interaction,ongoing research,unassigned 4,3,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31123811&form=6&db=m Nine novel HOGA1 gene mutations identified in primary hyperoxaluria type 3 and distinct clinical and biochemical characteristics in Chinese children. causal interaction,ongoing research,unassigned 3,1,0 4.1.3.16 4-hydroxy-2-oxoglutarate aldolase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22781098&form=6&db=m Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies. causal interaction,therapeutic application,unassigned 4,3,0 4.1.3.16 Hyperoxaluria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22781098&form=6&db=m Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies. causal interaction,therapeutic application,unassigned 4,3,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22781098&form=6&db=m Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies. causal interaction,therapeutic application,unassigned 4,3,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25629080&form=6&db=m Performance evaluation of Sanger sequencing for the diagnosis of primary hyperoxaluria and comparison with targeted next generation sequencing. therapeutic application,unassigned 1,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33948853&form=6&db=m Possible ethnic associations in primary hyperoxaluria type-III-associated HOGA1 sequence variants. ongoing research,unassigned 2,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21896830&form=6&db=m Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis. diagnostic usage,unassigned 3,0 4.1.3.16 Urolithiasis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21896830&form=6&db=m Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis. diagnostic usage,unassigned 3,0 4.1.3.16 4-hydroxy-2-oxoglutarate aldolase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22729392&form=6&db=m Primary hyperoxaluria type III-a model for studying perturbations in glyoxylate metabolism. causal interaction,unassigned 4,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22729392&form=6&db=m Primary hyperoxaluria type III-a model for studying perturbations in glyoxylate metabolism. causal interaction,unassigned 4,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22115483&form=6&db=m Re: Mutations in DHDPSL are Responsible for Primary Hyperoxaluria Type III. causal interaction,unassigned 4,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22325509&form=6&db=m Re: primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis. diagnostic usage,therapeutic application,unassigned 3,1,0 4.1.3.16 Urolithiasis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22325509&form=6&db=m Re: primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis. diagnostic usage,therapeutic application,unassigned 3,1,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31696211&form=6&db=m Regulation of human 4-hydroxy-2-oxoglutarate aldolase by pyruvate and ?-ketoglutarate: implications for primary hyperoxaluria type-3. ongoing research,therapeutic application,unassigned 2,1,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25972204&form=6&db=m Renal function can be impaired in children with primary hyperoxaluria type 3. causal interaction,unassigned 2,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21998747&form=6&db=m Structural and biochemical studies of human 4-hydroxy-2-oxoglutarate aldolase: implications for hydroxyproline metabolism in primary hyperoxaluria. diagnostic usage,ongoing research,unassigned 3,2,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22391140&form=6&db=m The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3. causal interaction,diagnostic usage,ongoing research,unassigned 4,3,2,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22851625&form=6&db=m The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type III. diagnostic usage,ongoing research,unassigned 3,2,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26340091&form=6&db=m Two Novel HOGA1 Splicing Mutations Identified in a Chinese Patient with Primary Hyperoxaluria Type 3. causal interaction,diagnostic usage,unassigned 3,1,0 4.1.3.16 Hyperoxaluria, Primary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32003182&form=6&db=m [Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder]. diagnostic usage,unassigned 1,0