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Disease Info Card
Chorea Acanthocytosis Syndrome
Information about Chorea Acanthocytosis Syndrome: 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 Chorea Acanthocytosis Syndrome
Most recent studies have shown that Chorea Acanthocytosis Syndrome shares some biological mechanisms with acanthocytosis, atrophy, behavioral-tic, blood-group-deletion-syndrome, chorea, dementia, dyskinetic-syndrome, dystonia-disorders, epilepsy, huntington-disease, involuntary-movements, movement-disorders, muscular-atrophy, myopathy, nerve-degeneration, nervous-system-disorder, nervousness, neurodegenerative-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Chorea Acanthocytosis Syndrome, and have been seen in publications frequently: Aging, Anion Transport, Cell Aging, Cell Death, Cytokinesis, Exocytosis, Localization, Mitochondrial Depolarization, Muscle Atrophy, Pathogenesis, Programmed Cell Death, Protein Phosphorylation, Reflex, Regulation Of Hormone Secretion, Segmentation, Sporulation, Sulfate Transport, Translation, Transport, Visual Perception
Quite a number of genes have been found to play important roles in Chorea Acanthocytosis Syndrome, such as ABCB4, ARNTL, ATN1, CHKA, CHKB, CP, GHRH, GNA14, HTT, JPH3, PANK2, SLC4A1, SLC6A4, TAC1, TBP, VPS13A, XK. 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.