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Disease Info Card
Hereditary Ataxia, Unspecified
Information about Hereditary Ataxia, Unspecified: 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 Hereditary Ataxia, Unspecified
Most recent studies have shown that Hereditary Ataxia, Unspecified shares some biological mechanisms with abnormal-degeneration, ataxia, ataxia-spinocerebellar, atrophy, cerebellar-ataxia, cerebellar-diseases, friedreich-ataxia, machado-joseph-disease, muscle-spasticity, muscular-atrophy, nervous-system-disorder, nervousness, neurodegenerative-disorders, olivopontocerebellar-atrophies, paraplegia, spastic-paraplegia, spinocerebellar-degeneration, trinucleotide-repeat-expansion.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hereditary Ataxia, Unspecified, and have been seen in publications frequently: Aging, Cell Death, Cognition, Dna Repair, Electron Transport, Glucose Homeostasis, Glycosylation, Hypersensitivity, Iron-sulfur Cluster Assembly, Localization, Mitochondrial Fusion, Muscle Atrophy, Oxidative Phosphorylation, Pathogenesis, Proprioception, Pyruvate Oxidation, Reflex, Translation, Transport, Tricarboxylic Acid Cycle
Quite a number of genes have been found to play important roles in Hereditary Ataxia, Unspecified, such as ATN1, ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A, FANCA, FXN, GAA, GLO1, GLUD1, LY6E, PDYN, PES1, PRKCG, SOD1, TBP, TRH. 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.