Pentanucleotide repeat expansions in the ATX2/SCA2 gene have been linked to spinocerebellar ataxia, a disorder that is characterized by gait ataxia, cognitive development, and seizures. The function of the ATX2/SCA2 has not been determined.
Alternative names for
SCA2/ATX2 Antibody include Ataxin-2 antibody,
ataxin 2 antibody,
Spinocerebellar ataxia type 2 protein antibody,
Trinucleotide repeat-containing gene 13 protein antibody,
trinucleotide repeat containing 13 antibody,
spinocerebellar ataxia type 2 protein antibody,
trinucleotide repeat-containing gene 13 protein antibody.