Research of Merrf Syndrome has been linked to Epilepsy, Epilepsies, Myoclonic, Melas Syndrome, Mitochondrial Diseases, Mitochondrial Encephalomyopathies. The study of Merrf Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Merrf Syndrome include Pathogenesis, Oxidative Phosphorylation, Translation, Transport, Mitochondrial Translation. These pathways complement our catalog of research reagents for the study of Merrf Syndrome including antibodies and ELISA kits against NEURONAL CEROID LIPOFUSCINOSIS, NAD(P)H DEHYDROGENASE (QUINONE), CDKN1A, COX8A, CPOX.
Merrf 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 Merrf Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 1260 products for the study of Merrf Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Merrf Syndrome is also known as merrf syndrome, merrf, myoclonic epilepsy associated with ragged-red fibers, myoencephalopathy ragged-red fiber disease, myoclonus with epilepsy and with ragged red fibers (merrf syndrome), myoclonic epilepsy associated with ragged red fibers, myoclonus epilepsy and ragged red fibers (disorder), myoclonic epilepsy - ragged red fibers (disorder), myoclonus with epilepsy with ragged red fibers, myoclonic epilepsy with ragged-red fibers, fukuhara syndrome (disorder), epilepsies, myoclonic, fukuhara syndrome, fukuhara disease.