Research of Ornithine Carbamoyltransferase Deficiency has been linked to Hyperammonemia, Urea Cycle Disorders, Inborn, Inborn Errors Of Metabolism, Comatose, Encephalopathies. The study of Ornithine Carbamoyltransferase Deficiency has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Ornithine Carbamoyltransferase Deficiency include Urea Cycle, Excretion, Transport, Pathogenesis, Fatty Acid Oxidation. These pathways complement our catalog of research reagents for the study of Ornithine Carbamoyltransferase Deficiency including antibodies and ELISA kits against SPARSE FUR, CPS, CARBAMYL PHOSPHATE SYNTHETASE I, AMINO-ACID N-ACETYLTRANSFERASE, ADSL.
Top Research Reagents
We have 1449 products for the study of Ornithine Carbamoyltransferase Deficiency that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Ornithine Carbamoyltransferase Deficiency is also known as ornithine carbamoyltransferase deficiency, ornithine transcarbamylase deficiency, otc deficiency, ornithine carbamoyltransferase deficiency disease, deficiency of citrulline phosphorylase, malnutrition, otcd.