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One of its most common hereditary forms, spinocerebellar ataxia type 3 (SCA3), stems from a genetic mutation in the ATXN3 gene and progressively damages the cerebellum

in the brain, it is synthesized in nonneuronal support cells and delivers cholesterol that neurons need to form membranes, synapses, and myelin

By using a liposomal delivery systemwhich involves wrapping the nutrient in a phospholipid bilayer (a protective fatty bubble that mirrors your cell membranes)we help ensure the Vitamin C reaches your cells

Safety, tolerability, and activity of ALXN1830 targeting the neonatal Fc receptor in chronic pemphigus

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