Research of Melas Syndrome has been linked to Acidosis, Lactic, Acidosis, Encephalopathies, Myopathy, Mitochondrial Myopathies. The study of Melas Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Melas Syndrome include Pathogenesis, Oxidative Phosphorylation, Translation, Transport, Mitochondrial Translation. These pathways complement our catalog of research reagents for the study of Melas Syndrome including antibodies and ELISA kits against CYCS, POLG, COX5A, CPOX, COX8A.
Melas Syndrome 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 Melas Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 1345 products for the study of Melas Syndrome that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Melas Syndrome is also known as melas syndrome, melas, mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes, myopathy, mitochondrial-encephalopathy-lactic acidosis-stroke, mitochondrial-encephalopathy-lactic acidosis-stroke, lactic acidosis,stroke-like episodes, myopathy, mitochondrial encephalomyopathies, mitochondrial encephalomyopathy, mitochondrial encephalopathy, mitochondrial myopathies, myopathy.
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