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Disease Info Card
Myokymia
Information about Myokymia: 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 Myokymia
Most recent studies have shown that Myokymia shares some biological mechanisms with ataxia, atrophy, chorea, diplopia, facial-myokymia, facial-nerve-diseases, isaacs-syndrome, movement-disorders, multiple-sclerosis, muscle-cramp, muscular-fasciculation, myoclonus, nystagmus, sclerosis, spasm, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Myokymia, and have been seen in publications frequently: Circadian Rhythm, Cognition, Dehiscence, Excretion, Flight, Hypersensitivity, Innervation, Localization, Membrane Depolarization, Muscle Atrophy, Muscle Contraction, Muscle Hypertrophy, Pathogenesis, Reflex, Regeneration, Secretion, Short-term Memory
Quite a number of genes have been found to play important roles in Myokymia, such as ADCY5, ATXN3, CACNA1A, CAMP, CD69, CSF2, GRHL3, KCNA1, KCNA2, KCNA4, KCNA6, KCNQ1, KCNQ2, KCNQ3, LAMC2, PMP22, PSMD1. 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.