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Disease Info Card
Mitochondrial Trifunctional Protein Deficiency
Information about Mitochondrial Trifunctional Protein Deficiency: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Mitochondrial Trifunctional Protein Deficiency
Most recent studies have shown that Mitochondrial Trifunctional Protein Deficiency shares some biological mechanisms with abetalipoproteinemia, acute-fatty-liver-of-pregnancy, cardiomyopathies, deficiency-of-3-hydroxyacyl-coa-dehydrogenase, fatty-liver, hellp-syndrome, hemolysis-(disorder), hypoglycemia, inborn-errors-of-metabolism, liver-diseases, metabolic-diseases, myopathy, pregnancy-complications, protein-deficiency, retinal-diseases, rhabdomyolysis, sudden-death.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mitochondrial Trifunctional Protein Deficiency, and have been seen in publications frequently: Cell Proliferation, Excretion, Fatty Acid Beta-oxidation, Fatty Acid Oxidation, Fatty Acid Transport, Lipid Storage, Localization, Long-chain Fatty Acid Transport, Mitochondrial Transport, Pathogenesis, Reverse Transcription, Translation, Transport
Quite a number of genes have been found to play important roles in Mitochondrial Trifunctional Protein Deficiency, such as ACADM, C12ORF57, CDH15, EHHADH, ERG, HADH, HADHA, HADHB, HSD17B10, KCNH2, LCN1, MT1B, MTTP, RPE, TMPO, TRIM39, TYMP. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.