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Disease Info Card
Mitochondrial Myopathy And Sideroblastic Anemia
Information about Mitochondrial Myopathy And Sideroblastic Anemia: 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 Myopathy And Sideroblastic Anemia
Most recent studies have shown that Mitochondrial Myopathy And Sideroblastic Anemia shares some biological mechanisms with acidemia, acidosis, acidosis-lactic, anemia, cytochrome-c-oxidase-deficiency, increased-metabolic-requirement, lactic-acidemia, liver-diseases, mitochondrial-diseases, mitochondrial-myopathies, myopathy, sideroblastic-anemia, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mitochondrial Myopathy And Sideroblastic Anemia, and have been seen in publications frequently: Mitochondrial Translation, Oxidative Phosphorylation, Pathogenesis, Translation, Trna Aminoacylation
Quite a number of genes have been found to play important roles in Mitochondrial Myopathy And Sideroblastic Anemia, such as APBB3, EP400, GALNT9, GFM1, MMP17, MSR1, PUS1, RARB, SFSWAP, SRA1, TRMU, ULK1, YARS2. 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.
Pathways Related to Mitochondrial Myopathy And Sideroblastic Anemia
This information is being compiled and will come in a future update
| Mitochondrial Translation | Oxidative Phosphorylation | Pathogenesis |
| Translation | Trna Aminoacylation |