Research of Hyperammonemia, Type Iii has been linked to Hyperammonemia, Urea Cycle Disorders, Inborn, Inborn Errors Of Metabolism, Comatose, Ornithine Carbamoyltransferase Deficiency. The study of Hyperammonemia, Type Iii has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hyperammonemia, Type Iii include Urea Cycle, Translation, Localization, Excretion. These pathways complement our catalog of research reagents for the study of Hyperammonemia, Type Iii including antibodies and ELISA kits against NAGS, AMINO-ACID N-ACETYLTRANSFERASE, SCN7A, NBAS, NAGLU.
Hyperammonemia, Type Iii Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Hyperammonemia, Type Iii below!
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We have 858 products for the study of Hyperammonemia, Type Iii that can be applied to Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Hyperammonemia, Type Iii is also known as Aga Deficiency, N-acetyl Glutamate Synthetase Deficiency, N-acetylglutamate Synthase Deficiency, N-acetylglutamate Synthetase Deficiency, Nags Deficiency.