Research of Hmg Coa Lyase Deficiency has been linked to Inborn Errors Of Metabolism, Acidosis, Hypoglycemia, Metabolic Acidosis, Methylmalonic Acidemia. The study of Hmg Coa Lyase Deficiency has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hmg Coa Lyase Deficiency include Excretion, Fatty Acid Oxidation, Urea Cycle, Methylation, Transport. These pathways complement our catalog of research reagents for the study of Hmg Coa Lyase Deficiency including antibodies and ELISA kits against HMGCL, 3-HYDROXY-3-METHYLGLUTARYL-COENZYME A LYASE, HES1, LIPC, MEDIUM-CHAIN ACYL-COA DEHYDROGENASE.
Hmg Coa Lyase Deficiency 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 Hmg Coa Lyase Deficiency below!
For more information on how to use Laverne, please read the How to Guide.
We have 755 products for the study of Hmg Coa Lyase Deficiency that can be applied to Chromatin Immunoprecipitation, Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Hmg Coa Lyase Deficiency is also known as hmg-coa lyase deficiency, 3-hydroxy-3-methylglutaryl-coa lyase deficiency, hydroxymethylglutaric aciduria, hmg coa lyase deficiency, 3-hydroxy-3-methylglutaryl-coenzyme a lyase deficiency, deficiency of hydroxymethylglutaryl-coa lyase, 3-hydroxy-3-methylglutaric aciduria, 3-oh 3-methyl glutaric aciduria, defect in leucine metabolism, 3-oh 3-ch3 glutaric aciduria, hl deficiency, 3hmg, hmg.
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