Pages that link to "Q68157126"
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The following pages link to Dihydropyrimidinuria (Q68157126):
Displaying 15 items.
- A novel gene family defined by human dihydropyrimidinase and three related proteins with differential tissue distribution (Q24308901) (← links)
- Dihydropyrimidinase deficiency: structural organization, chromosomal localization, and mutation analysis of the human dihydropyrimidinase gene (Q24336851) (← links)
- Genetic polymorphisms of dihydropyrimidinase in a Japanese patient with capecitabine-induced toxicity (Q28546743) (← links)
- Clinical, biochemical and genetic findings in two siblings with a dihydropyrimidinase deficiency. (Q34612087) (← links)
- Altered Pre-mRNA Splicing Caused by a Novel Intronic Mutation c.1443 5G>A in the Dihydropyrimidinase (DPYS) Gene (Q35895211) (← links)
- Inborn errors of purine and pyrimidine metabolism. (Q37416449) (← links)
- Inborn errors of pyrimidine degradation: Clinical, biochemical and molecular aspects (Q41521423) (← links)
- Inherited defects of purine and pyrimidine metabolism: Laboratory methods for diagnosis (Q41521436) (← links)
- Dihydropyridmidinase deficiency and congenital microvillous atrophy: Coincidence or genetic relation? (Q42547285) (← links)
- Dihydropyrimidinase deficiency: the first feline case of dihydropyrimidinuria with clinical and molecular findings (Q43186153) (← links)
- Screening for defects of dihydropyrimidine degradation by analysis of amino acids in urine before and after acid hydrolysis (Q67560174) (← links)
- Simple Method for the Quantitative Analysis of Dihydropyrimidines and N-Carbamyl-ß-Amino Acids in Urine (Q67838689) (← links)
- Dihydropyrimidinuria without clinical symptoms (Q71726889) (← links)
- Clinical and biochemical findings in six patients with pyrimidine degradation defects (Q72110058) (← links)
- Clinical and Biochemical Aspects of Dihydropyrimidinase Deficiency (Q74580781) (← links)