Spinocerebellar Ataxia, Autosomal Recessive 1

Overview of Spinocerebellar Ataxia, Autosomal Recessive 1

Most recent studies have shown that Spinocerebellar Ataxia, Autosomal Recessive 1 shares some biological mechanisms with amyotrophic-lateral-sclerosis, apraxias, ataxia, cerebellar-ataxia, dysarthria, dysequilibrium-syndrome, infectious-bovine-keratoconjunctivitis, infective-disorder, motor-neuron-disease, muscular-atrophy, neoplasms, ocular-motility-disorders, oculomotor-apraxia, oculomotor-nerve-paralysis, plant-diseases, primary-lateral-sclerosis, sclerosis, tissue-adhesions, wiskott-aldrich-syndrome.

Among the many pathways, these few ones have gauged particular interests from scientists studying Spinocerebellar Ataxia, Autosomal Recessive 1, and have been seen in publications frequently: Actin Nucleation, Cell Growth, Cell Migration, Cell Morphogenesis, Cell Motility, Localization, Locomotion, Neuron Death, Ruffle Assembly, Virulence, Wound Healing

Quite a number of genes have been found to play important roles in Spinocerebellar Ataxia, Autosomal Recessive 1, such as ACTR2, ACTR3, AFP, AICDA, ANGPTL2, APOBEC3A, BRK1, ENAH, PXN, RPS4X, SETX, SRC, TRIM26, VASP, VCL, WAS, WASF1, WASF2, WASF3, WASL. 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.

Spinocerebellar Ataxia, Autosomal Recessive 1 Related Genes

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Pathways Related to Spinocerebellar Ataxia, Autosomal Recessive 1

This information is being compiled and will come in a future update

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