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Disease Info Card
Dystonia, Primary
Information about Dystonia, Primary: 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 Dystonia, Primary
Most recent studies have shown that Dystonia, Primary shares some biological mechanisms with blepharospasm, depressive-disorder, dyskinetic-syndrome, dystonia-disorders, dystonia-musculorum-deformans, focal-dystonia, generalized-dystonia, globus-hystericus, involuntary-movements, movement-disorders, muscle-cramp, myoclonus, organic-writers-cramp, pain, parkinson-disease, secondary-dystonia, secondary-parkinson-disease, torticollis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Dystonia, Primary, and have been seen in publications frequently: Brain Development, Cell Cycle, Cell Proliferation, Cognition, Endocytosis, Exocytosis, Exogen, Habituation, Localization, Locomotion, Muscle Contraction, Myelination, Pathogenesis, Reflex, Response To Amphetamine, Segmentation, Sensory Processing, Startle Response, Synaptic Vesicle Endocytosis, Transport
Quite a number of genes have been found to play important roles in Dystonia, Primary, such as ATP1A3, BDNF, CAMP, CIZ1, EEF1A2, GCH1, LRP2, MCF2L, MERTK, PNKD, PRKRA, SGCE, SLC2A1, SLC6A3, TAF1, TH, THAP1, TOR1A. 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.